Ignite Creation Date:
2025-12-24 @ 10:57 PM
Ignite Modification Date:
2025-12-31 @ 2:24 AM
Study NCT ID:
NCT01200069
Status:
TERMINATED
Last Update Posted:
2017-03-29
First Post:
2010-08-19
Is NOT Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
IV Ibuprofen for Post-Electroconvulsive Therapy Myalgia
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D003863', 'term': 'Depression'}, {'id': 'D063806', 'term': 'Myalgia'}], 'ancestors': [{'id': 'D001526', 'term': 'Behavioral Symptoms'}, {'id': 'D001519', 'term': 'Behavior'}, {'id': 'D009135', 'term': 'Muscular Diseases'}, {'id': 'D009140', 'term': 'Musculoskeletal Diseases'}, {'id': 'D009468', 'term': 'Neuromuscular Diseases'}, {'id': 'D009422', 'term': 'Nervous System Diseases'}, {'id': 'D059352', 'term': 'Musculoskeletal Pain'}, {'id': 'D010146', 'term': 'Pain'}, {'id': 'D009461', 'term': 'Neurologic Manifestations'}, {'id': 'D012816', 'term': 'Signs and Symptoms'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D000077325', 'term': "Ringer's Lactate"}, {'id': 'D007052', 'term': 'Ibuprofen'}], 'ancestors': [{'id': 'D000077324', 'term': 'Crystalloid Solutions'}, {'id': 'D007552', 'term': 'Isotonic Solutions'}, {'id': 'D012996', 'term': 'Solutions'}, {'id': 'D004364', 'term': 'Pharmaceutical Preparations'}, {'id': 'D010666', 'term': 'Phenylpropionates'}, {'id': 'D000146', 'term': 'Acids, Carbocyclic'}, {'id': 'D002264', 'term': 'Carboxylic Acids'}, {'id': 'D009930', 'term': 'Organic Chemicals'}]}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'tilakva@njms.rutgers.edu', 'phone': '974 972-5254', 'title': 'Vasanti Tilak, MD', 'organization': 'Rutgers/New Jersey Medical School'}, 'certainAgreement': {'piSponsorEmployee': True}}, 'adverseEventsModule': {'timeFrame': '0-72 hours after each of the 3 treatments', 'description': 'treatment day 1 at 1 hour post ECT procedure subject experienced dizziness\n\ntreatment day 3 at 6 hour post procedure subject reported dizziness', 'eventGroups': [{'id': 'EG000', 'title': 'Sugar Water', 'description': '500 mL of ringers lactate over 30 minutes to be administered prior to ECT for treatments 1,2 and 3\n\nPlacebo infusion: Identically appearing placebo dose administered IV prior to ECT and subsequently on ECT treatments 2 and 3', 'otherNumAtRisk': 8, 'otherNumAffected': 2, 'seriousNumAtRisk': 8, 'seriousNumAffected': 0}, {'id': 'EG001', 'title': 'Ibuprofen', 'description': '800mg/8mL of intravenous ibuprofen over 30 min in 500mL of ringers lactate to be administered prior to ECT for treatments # 1, 2 and 3\n\nibuprofen intravenous: IV ibuprofen 800mg/8ml given over 30 minutes prior to ECT and subsequently on ECT treatments 2 and 3', 'otherNumAtRisk': 6, 'otherNumAffected': 1, 'seriousNumAtRisk': 6, 'seriousNumAffected': 0}], 'otherEvents': [{'term': 'dizzyness', 'stats': [{'groupId': 'EG000', 'numAtRisk': 8, 'numAffected': 2}, {'groupId': 'EG001', 'numAtRisk': 6, 'numAffected': 0}], 'organSystem': 'Nervous system disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'vertigo'}, {'term': 'vomiting', 'stats': [{'groupId': 'EG000', 'numAtRisk': 8, 'numAffected': 0}, {'groupId': 'EG001', 'numAtRisk': 6, 'numAffected': 1}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'nausea'}], 'frequencyThreshold': '3'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'PRIMARY', 'title': 'Subject Self Reported Numerical Rating of Incidence and Severity of Post-Electroconvulsive Therapy Myalgias After Treatment 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '8', 'groupId': 'OG000'}, {'value': '6', 'groupId': 'OG001'}, {'value': '8', 'groupId': 'OG002'}, {'value': '6', 'groupId': 'OG003'}, {'value': '8', 'groupId': 'OG004'}, {'value': '6', 'groupId': 'OG005'}, {'value': '8', 'groupId': 'OG006'}, {'value': '6', 'groupId': 'OG007'}]}], 'groups': [{'id': 'OG000', 'title': 'Sugar Water-one Hour After Treatment #1', 'description': '500 mL of ringers lactate over 30 minutes to be administered prior to ECT for treatment 1, at one hour following procedure'}, {'id': 'OG001', 'title': 'Ibuprofen One Hour After Treatment #1', 'description': '800mg/8mL of intravenous ibuprofen over 30 min in 500mL of ringers lactate to be administered prior to ECT for treatments # 1, 2 and 3\n\nsubject report of myalgia one hour after completion of procedure number 1'}, {'id': 'OG002', 'title': 'Sugar Water 6 Hours After Procedure #1', 'description': 'Subject reported myalgia 6 hours after completion of treatment # 1,'}, {'id': 'OG003', 'title': 'Ibuprofen 6 Hours After Treatment #1', 'description': 'subject reported myalgia 6 hours after treatment 1'}, {'id': 'OG004', 'title': 'Sugar Water 24 Hours After Treatment #1', 'description': 'subject reported myalgia 24 hours after completion of procedure 1'}, {'id': 'OG005', 'title': 'Ibuprofen 24 Hours After Treatment 1', 'description': 'subject reported myalgia 24 hours after procedure 1'}, {'id': 'OG006', 'title': 'Sugar Water 48 Hours After Procedure 1', 'description': 'subject reported myalgia 48 hours after procedure 1'}, {'id': 'OG007', 'title': 'Ibuprofen 48 Hours After Treatment 1', 'description': 'subject reported myalgia 48 hours after treatment day 1'}], 'classes': [{'categories': [{'measurements': [{'value': '2', 'groupId': 'OG000', 'lowerLimit': '0', 'upperLimit': '4'}, {'value': '0', 'groupId': 'OG001', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '7.5', 'groupId': 'OG002', 'lowerLimit': '5', 'upperLimit': '10'}, {'value': '1.5', 'groupId': 'OG003', 'lowerLimit': '0', 'upperLimit': '3'}, {'value': '2.5', 'groupId': 'OG004', 'lowerLimit': '2', 'upperLimit': '5'}, {'value': '.5', 'groupId': 'OG005', 'lowerLimit': '0', 'upperLimit': '1'}, {'value': '0', 'groupId': 'OG006', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG007', 'lowerLimit': '0', 'upperLimit': '0'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Treatment day 1 at 1hour, 6 hour, 24 hours, 48 hours', 'description': 'subject self reporting rating scale for severity of myalgias utilizing numeric rating scale 0= no pain, 1-3= mild pain, annoyance with little interference with Activities of Daily Living (ADL), 4-6= moderate (interferes significantly with ADL, 7-10 = severe pain unable to perform ADL', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Full Range', 'reportingStatus': 'POSTED', 'populationDescription': 'subjects report at one hour following treatment'}, {'type': 'PRIMARY', 'title': 'Myalgia Reported on Treatment Day 2', 'denoms': [{'units': 'Participants', 'counts': [{'value': '8', 'groupId': 'OG000'}, {'value': '5', 'groupId': 'OG001'}, {'value': '8', 'groupId': 'OG002'}, {'value': '5', 'groupId': 'OG003'}, {'value': '8', 'groupId': 'OG004'}, {'value': '5', 'groupId': 'OG005'}, {'value': '8', 'groupId': 'OG006'}, {'value': '5', 'groupId': 'OG007'}]}], 'groups': [{'id': 'OG000', 'title': 'Sugar Water-one Hour After Treatment 2', 'description': '500 mL of ringers lactate over 30 minutes to be administered prior to ECT for treatments 2\n\nPlacebo infusion: Identically appearing placebo dose administered IV prior to ECT and subsequently on ECT treatment day 2'}, {'id': 'OG001', 'title': 'Ibuprofen One Hour After Treatment #2', 'description': '800mg/8mL of intravenous ibuprofen over 30 min in 500mL of ringers lactate to be administered prior to ECT for treatments # 2 one hour after treatment\n\nibuprofen intravenous: IV ibuprofen 800mg/8ml given over 30 minutes prior to ECT treatment day 2'}, {'id': 'OG002', 'title': 'Sugar Water 6 Hours After Procedure #2', 'description': 'Subject reported myalgia 6 hours after completion of treatment #2'}, {'id': 'OG003', 'title': 'Ibuprofen 6 Hours After Treatment #2', 'description': 'Subject reported myalgia 6 hours after completion of treatment #2'}, {'id': 'OG004', 'title': 'Sugar Water 24 Hours After Treatment #2', 'description': 'Subject reported myalgia 24 hours after completion of treatment #2'}, {'id': 'OG005', 'title': 'Ibuprofen 24 Hours After Treatment #2', 'description': 'Subject reported myalgia 24 hours after completion of treatment #2'}, {'id': 'OG006', 'title': 'Sugar Water 48 Hours After Treatment 2', 'description': 'Subject reported myalgia 48 hours after completion of treatment #2'}, {'id': 'OG007', 'title': 'Ibuprofen 48 Hours After Treatment 2', 'description': 'Subject reported myalgia 48 hours after completion of treatment #2'}], 'classes': [{'categories': [{'measurements': [{'value': '1.5', 'groupId': 'OG000', 'lowerLimit': '0', 'upperLimit': '3'}, {'value': '0', 'groupId': 'OG001', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG002', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '1.5', 'groupId': 'OG003', 'lowerLimit': '0', 'upperLimit': '3'}, {'value': '0', 'groupId': 'OG004', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG005', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG006', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG007', 'lowerLimit': '0', 'upperLimit': '0'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': '1 hour, 6 hours, 24 hours & 48 hours following procedure', 'description': 'Subject self reported numerical rating of incidence and severity of post ECT Myalgia after treatment day 2 0=no pain, 1-3=mild pain (annoying, little interference with ADL), 4-6= moderate,( interferes significantly with ADL) 7-10 severe pain (unable to perform everyday activities)', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Full Range', 'reportingStatus': 'POSTED'}, {'type': 'PRIMARY', 'title': 'Myalgia Reported After Treatment #3', 'denoms': [{'units': 'Participants', 'counts': [{'value': '8', 'groupId': 'OG000'}, {'value': '5', 'groupId': 'OG001'}, {'value': '8', 'groupId': 'OG002'}, {'value': '5', 'groupId': 'OG003'}, {'value': '8', 'groupId': 'OG004'}, {'value': '5', 'groupId': 'OG005'}, {'value': '8', 'groupId': 'OG006'}, {'value': '7', 'groupId': 'OG007'}]}], 'groups': [{'id': 'OG000', 'title': 'Sugar Water-one Hour After Treatment 3', 'description': '500 mL of ringers lactate over 30 minutes to be administered prior to ECT for treatments 3\n\nPlacebo infusion: Identically appearing placebo dose administered IV prior to ECT and subsequently on ECT treatment day 2'}, {'id': 'OG001', 'title': 'Ibuprofen One Hour After Treatment #3', 'description': '800mg/8mL of intravenous ibuprofen over 30 min in 500mL of ringers lactate to be administered prior to ECT for treatments # 3 one hour after treatment\n\nibuprofen intravenous: IV ibuprofen 800mg/8ml given over 30 minutes prior to ECT treatment day 2'}, {'id': 'OG002', 'title': 'Sugar Water 6 Hours After Procedure #3', 'description': 'Subject reported myalgia 6 hours after completion of treatment #3'}, {'id': 'OG003', 'title': 'Ibuprofen 6 Hours After Treatment #3', 'description': 'Subject reported myalgia 6 hours after completion of treatment #3'}, {'id': 'OG004', 'title': 'Sugar Water 24 Hours After Treatment #3', 'description': 'Subject reported myalgia 24 hours after completion of treatment #3'}, {'id': 'OG005', 'title': 'Ibuprofen 24 Hours After Treatment #3', 'description': 'Subject reported myalgia 24 hours after completion of treatment #3'}, {'id': 'OG006', 'title': 'Sugar Water 48 Hours After Treatment 3', 'description': 'Subject reported myalgia 48 hours after completion of treatment #3'}, {'id': 'OG007', 'title': 'Ibuprofen 48 Hours After Treatment 3', 'description': 'Subject reported myalgia 48 hours after completion of treatment #3'}], 'classes': [{'categories': [{'measurements': [{'value': '0', 'groupId': 'OG000', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG001', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG002', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG003', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG004', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG005', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG006', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG007', 'lowerLimit': '0', 'upperLimit': '0'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': '1 hour, 6 hour, 24 hour, 48 hour after 3rd ECT treatment', 'description': 'Subject self reported severity of myalgia based on a self reported assessment utilizing numeric rating scale 0=no myalgia, 1-3=mild myalgia (annoying, little interference with ADL);4-6=moderate (interferes significantly with ADL); 7-10 severe myalgia(unable to perform every day activities)', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Full Range', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Subject Self Reported Numerical Rating of Incidence and Severity of Post Electroconvulsive Therapy Headache After Treatment Day 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '8', 'groupId': 'OG000'}, {'value': '6', 'groupId': 'OG001'}, {'value': '8', 'groupId': 'OG002'}, {'value': '6', 'groupId': 'OG003'}, {'value': '8', 'groupId': 'OG004'}, {'value': '6', 'groupId': 'OG005'}, {'value': '8', 'groupId': 'OG006'}, {'value': '6', 'groupId': 'OG007'}]}], 'groups': [{'id': 'OG000', 'title': 'Pain Score Sugar Water-one Hour After Treatment 1', 'description': '500 mL of ringers lactate over 30 minutes to be administered prior to ECT for treatments 1\n\nPlacebo infusion: Identically appearing placebo dose administered IV prior to ECT and subsequently on ECT treatment day 1'}, {'id': 'OG001', 'title': 'Pain Score Ibuprofen One Hour After Treatment #1', 'description': '800mg/8mL of intravenous ibuprofen over 30 min in 500mL of ringers lactate to be administered prior to ECT for treatments # 1 one hour after treatment\n\nibuprofen intravenous: IV ibuprofen 800mg/8ml given over 30 minutes prior to ECT treatment day 2'}, {'id': 'OG002', 'title': 'Pain Score After Sugar Water 6 Hours After Treatment #1', 'description': 'Subject reported headache 6 hours after completion of treatment #1'}, {'id': 'OG003', 'title': 'Pain Score Ibuprofen 6 Hours After Treatment #1', 'description': 'Subject reported headache 6 hours after completion of treatment #1'}, {'id': 'OG004', 'title': 'Pain Score Sugar Water 24 Hours After Treatment #1', 'description': 'Subject reported headache 24 hours after completion of treatment #1'}, {'id': 'OG005', 'title': 'Pain Score Ibuprofen 24 Hours After Treatment #1', 'description': 'Subjects reported headache 24 hours after completion of treatment #1'}, {'id': 'OG006', 'title': 'Pain Score Sugar Water 48 Hours After Treatment 1', 'description': 'Subjects reported headache 48 hours after completion of treatment #1'}, {'id': 'OG007', 'title': 'Pain Score Ibuprofen 48 Hours After Treatment 1', 'description': 'Subjects reported headache 48 hours after completion of treatment #1'}], 'classes': [{'categories': [{'measurements': [{'value': '2.6', 'groupId': 'OG000', 'lowerLimit': '0', 'upperLimit': '6'}, {'value': '1.5', 'groupId': 'OG001', 'lowerLimit': '0', 'upperLimit': '5'}, {'value': '3.1', 'groupId': 'OG002', 'lowerLimit': '3', 'upperLimit': '10'}, {'value': '1.3', 'groupId': 'OG003', 'lowerLimit': '0', 'upperLimit': '4'}, {'value': '3.6', 'groupId': 'OG004', 'lowerLimit': '0', 'upperLimit': '5'}, {'value': '.16', 'groupId': 'OG005', 'lowerLimit': '0', 'upperLimit': '1'}, {'value': '0', 'groupId': 'OG006', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG007', 'lowerLimit': '0', 'upperLimit': '0'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 hour, 6 hours, 24 hours & 48 hours following procedure', 'description': 'Subject self reported numerical rating of incidence and severity of Post ECT pain score for headache at 1, 6, 24 and 48 hours post procedure. Pain Rating 0= no pain, 2-4=moderate pain, 5-7=distressing severe pain, 8-9=intense very severe pain, 10=unbearable pain', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Full Range', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Incidence and Severity of Headache After ECT Treatment 2', 'denoms': [{'units': 'Participants', 'counts': [{'value': '8', 'groupId': 'OG000'}, {'value': '5', 'groupId': 'OG001'}, {'value': '8', 'groupId': 'OG002'}, {'value': '5', 'groupId': 'OG003'}, {'value': '8', 'groupId': 'OG004'}, {'value': '8', 'groupId': 'OG005'}, {'value': '7', 'groupId': 'OG006'}, {'value': '8', 'groupId': 'OG007'}]}], 'groups': [{'id': 'OG000', 'title': 'Sugar Water-one Hour After Treatment 2', 'description': '500 mL of ringers lactate over 30 minutes to be administered prior to ECT for treatments 2\n\nPlacebo infusion: Identically appearing placebo dose administered IV prior to ECT and subsequently on ECT treatment day 2'}, {'id': 'OG001', 'title': 'Ibuprofen One Hour After Treatment #2', 'description': '800mg/8mL of intravenous ibuprofen over 30 min in 500mL of ringers lactate to be administered prior to ECT for treatments #2 one hour after treatment\n\nibuprofen intravenous: IV ibuprofen 800mg/8ml given over 30 minutes prior to ECT treatment day 2'}, {'id': 'OG002', 'title': 'Sugar Water 6 Hours After Procedure #2', 'description': 'Subject reported headache 6 hours after completion of treatment #2'}, {'id': 'OG003', 'title': 'Ibuprofen 6 Hours After Treatment #2', 'description': 'Subject reported headache 6 hours after completion of treatment #2'}, {'id': 'OG004', 'title': 'Sugar Water 24 Hours After Treatment #2', 'description': 'Subject reported headache 24 hours after completion of treatment #2'}, {'id': 'OG005', 'title': 'Ibuprofen 24 Hours After Treatment #2', 'description': 'Subject reported headache 24 hours after completion of treatment #2'}, {'id': 'OG006', 'title': 'Sugar Water 48 Hours After Treatment #2', 'description': 'Subject reported headache 48 hours after completion of treatment #2'}, {'id': 'OG007', 'title': 'Ibuprofen 48 Hours After Treatment #2', 'description': 'Subject reported headache 48 hours after completion of treatment #2'}], 'classes': [{'categories': [{'measurements': [{'value': '1.4', 'groupId': 'OG000', 'lowerLimit': '0', 'upperLimit': '5'}, {'value': '1.1', 'groupId': 'OG001', 'lowerLimit': '0', 'upperLimit': '4'}, {'value': '1.55', 'groupId': 'OG002', 'lowerLimit': '0', 'upperLimit': '5'}, {'value': '1', 'groupId': 'OG003', 'lowerLimit': '0', 'upperLimit': '5'}, {'value': '.18', 'groupId': 'OG004', 'lowerLimit': '0', 'upperLimit': '2'}, {'value': '.14', 'groupId': 'OG005', 'lowerLimit': '0', 'upperLimit': '1'}, {'value': '0', 'groupId': 'OG006', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '.14', 'groupId': 'OG007', 'lowerLimit': '0', 'upperLimit': '1'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 hour, 6 hour, 24 hour and 48 hours', 'description': 'Subject self reported numerical rating of incidence and severity of post ECT headache 0=no pain, 2-4=moderate pain, 5-7= distressing severe pain, 8-9= very severe pain, 10=unbearable pain.', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Full Range', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Incidence of Headache & Severity Headache After ECT Treatment #3', 'denoms': [{'units': 'Participants', 'counts': [{'value': '8', 'groupId': 'OG000'}, {'value': '5', 'groupId': 'OG001'}, {'value': '8', 'groupId': 'OG002'}, {'value': '5', 'groupId': 'OG003'}, {'value': '8', 'groupId': 'OG004'}, {'value': '5', 'groupId': 'OG005'}, {'value': '8', 'groupId': 'OG006'}, {'value': '5', 'groupId': 'OG007'}]}], 'groups': [{'id': 'OG000', 'title': 'Sugar Water-one Hour After Treatment 3', 'description': '500 mL of ringers lactate over 30 minutes to be administered prior to ECT for treatments 3\n\nPlacebo infusion: Identically appearing placebo dose administered IV prior to ECT and subsequently on ECT treatment day 2'}, {'id': 'OG001', 'title': 'Ibuprofen One Hour After Treatment #3', 'description': '800mg/8mL of intravenous ibuprofen over 30 min in 500mL of ringers lactate to be administered prior to ECT for treatments # 3 one hour after treatment\n\nibuprofen intravenous: IV ibuprofen 800mg/8ml given over 30 minutes prior to ECT treatment day 2'}, {'id': 'OG002', 'title': 'Sugar Water 6 Hours After Procedure #3', 'description': 'Subject reported headache 6 hours after completion of treatment #3'}, {'id': 'OG003', 'title': 'Ibuprofen 6 Hours After Treatment #3', 'description': 'Subject reported headache 6 hours after completion of treatment #3'}, {'id': 'OG004', 'title': 'Sugar Water 24 Hours After Treatment #3', 'description': 'Subject reported headache 24 hours after completion of treatment #3'}, {'id': 'OG005', 'title': 'Ibuprofen 24 Hours After Treatment #3', 'description': 'Subject reported headache 24 hours after completion of treatment #3'}, {'id': 'OG006', 'title': 'Sugar Water 48 Hours After Treatment 3', 'description': 'Subject reported headache 48 hours after completion of treatment #3'}, {'id': 'OG007', 'title': 'Ibuprofen 48 Hours After Treatment 3', 'description': 'Subject reported headache 48 hours after completion of treatment #3'}], 'classes': [{'categories': [{'measurements': [{'value': '0', 'groupId': 'OG000', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '.64', 'groupId': 'OG001', 'lowerLimit': '0', 'upperLimit': '4'}, {'value': '.28', 'groupId': 'OG002', 'lowerLimit': '0', 'upperLimit': '2'}, {'value': '1', 'groupId': 'OG003', 'lowerLimit': '0', 'upperLimit': '6'}, {'value': '0', 'groupId': 'OG004', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '.16', 'groupId': 'OG005', 'lowerLimit': '0', 'upperLimit': '1'}, {'value': '0', 'groupId': 'OG006', 'lowerLimit': '0', 'upperLimit': '0'}, {'value': '0', 'groupId': 'OG007', 'lowerLimit': '0', 'upperLimit': '0'}]}]}], 'paramType': 'MEAN', 'timeFrame': '1 hour after treatment, 6 hours, 24 hours and 48 hours', 'description': 'Subject self reported numerical rating of incidence and severity of post ECT headache after treatment #3, 0=no pain, 2-4=moderate pain, 5-7=distressing severe pain, 8-9 very serious pain, 10=unbearable pain.', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Full Range', 'reportingStatus': 'POSTED'}]}, 'participantFlowModule': {'groups': [{'id': 'FG000', 'title': 'Sugar Water', 'description': '500 mL of ringers lactate over 30 minutes to be administered prior to ECT for treatments 1,2 and 3\n\nPlacebo infusion: Identically appearing placebo dose administered IV prior to ECT and subsequently on ECT treatments 2 and 3'}, {'id': 'FG001', 'title': 'Ibuprofen', 'description': '800mg/8mL of intravenous ibuprofen over 30 min in 500mL of ringers lactate to be administered prior to ECT for treatments # 1, 2 and 3\n\nibuprofen intravenous: IV ibuprofen 800mg/8ml given over 30 minutes prior to ECT and subsequently on ECT treatments 2 and 3'}], 'periods': [{'title': 'Overall Study', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '8'}, {'groupId': 'FG001', 'numSubjects': '6'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '8'}, {'groupId': 'FG001', 'numSubjects': '5'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '1'}]}], 'dropWithdraws': [{'type': 'Withdrawal by Subject', 'reasons': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '1'}]}]}], 'recruitmentDetails': 'recruited following assigned schedule date and time for first ECT treatment, Procedure took place in Medical Special procedure unit (same day service)'}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '8', 'groupId': 'BG000'}, {'value': '6', 'groupId': 'BG001'}, {'value': '14', 'groupId': 'BG002'}]}], 'groups': [{'id': 'BG000', 'title': 'Sugar Water', 'description': '500 mL of ringers lactate over 30 minutes to be administered prior to ECT for treatments 1,2 and 3\n\nPlacebo infusion: Identically appearing placebo dose administered IV prior to ECT and subsequently on ECT treatments 2 and 3'}, {'id': 'BG001', 'title': 'Ibuprofen', 'description': '800mg/8mL of intravenous ibuprofen over 30 min in 500mL of ringers lactate to be administered prior to ECT for treatments # 1, 2 and 3\n\nibuprofen intravenous: IV ibuprofen 800mg/8ml given over 30 minutes prior to ECT and subsequently on ECT treatments 2 and 3'}, {'id': 'BG002', 'title': 'Total', 'description': 'Total of all reporting groups'}], 'measures': [{'title': 'Age, Categorical', 'classes': [{'categories': [{'title': '<=18 years', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'Between 18 and 65 years', 'measurements': [{'value': '8', 'groupId': 'BG000'}, {'value': '5', 'groupId': 'BG001'}, {'value': '13', 'groupId': 'BG002'}]}, {'title': '>=65 years', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '1', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '5', 'groupId': 'BG000'}, {'value': '4', 'groupId': 'BG001'}, {'value': '9', 'groupId': 'BG002'}]}, {'title': 'Male', 'measurements': [{'value': '3', 'groupId': 'BG000'}, {'value': '2', 'groupId': 'BG001'}, {'value': '5', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Region of Enrollment', 'classes': [{'title': 'United States', 'categories': [{'measurements': [{'value': '8', 'groupId': 'BG000'}, {'value': '6', 'groupId': 'BG001'}, {'value': '14', 'groupId': 'BG002'}]}]}], 'paramType': 'NUMBER', 'unitOfMeasure': 'participants'}, {'title': 'Mini Mental State Examination >23', 'classes': [{'categories': [{'measurements': [{'value': '8', 'groupId': 'BG000'}, {'value': '6', 'groupId': 'BG001'}, {'value': '14', 'groupId': 'BG002'}]}]}], 'paramType': 'NUMBER', 'description': 'examination of participants to confirm cognitive ability. Questions such as who is the president, what is the day of the week, the date. The scale is from 0-30. Value of 24 or higher indicates absence of cognitive impairment', 'unitOfMeasure': 'participants'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE4'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'DOUBLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 14}}, 'statusModule': {'whyStopped': 'unable to increase to target enrollment', 'overallStatus': 'TERMINATED', 'startDateStruct': {'date': '2010-07'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2015-03', 'completionDateStruct': {'date': '2014-09', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2017-02-27', 'studyFirstSubmitDate': '2010-08-19', 'resultsFirstSubmitDate': '2016-02-24', 'studyFirstSubmitQcDate': '2010-09-09', 'lastUpdatePostDateStruct': {'date': '2017-03-29', 'type': 'ACTUAL'}, 'resultsFirstSubmitQcDate': '2016-09-27', 'studyFirstPostDateStruct': {'date': '2010-09-13', 'type': 'ESTIMATED'}, 'resultsFirstPostDateStruct': {'date': '2016-11-18', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2014-09', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Subject Self Reported Numerical Rating of Incidence and Severity of Post-Electroconvulsive Therapy Myalgias After Treatment 1', 'timeFrame': 'Treatment day 1 at 1hour, 6 hour, 24 hours, 48 hours', 'description': 'subject self reporting rating scale for severity of myalgias utilizing numeric rating scale 0= no pain, 1-3= mild pain, annoyance with little interference with Activities of Daily Living (ADL), 4-6= moderate (interferes significantly with ADL, 7-10 = severe pain unable to perform ADL'}, {'measure': 'Myalgia Reported on Treatment Day 2', 'timeFrame': '1 hour, 6 hours, 24 hours & 48 hours following procedure', 'description': 'Subject self reported numerical rating of incidence and severity of post ECT Myalgia after treatment day 2 0=no pain, 1-3=mild pain (annoying, little interference with ADL), 4-6= moderate,( interferes significantly with ADL) 7-10 severe pain (unable to perform everyday activities)'}, {'measure': 'Myalgia Reported After Treatment #3', 'timeFrame': '1 hour, 6 hour, 24 hour, 48 hour after 3rd ECT treatment', 'description': 'Subject self reported severity of myalgia based on a self reported assessment utilizing numeric rating scale 0=no myalgia, 1-3=mild myalgia (annoying, little interference with ADL);4-6=moderate (interferes significantly with ADL); 7-10 severe myalgia(unable to perform every day activities)'}], 'secondaryOutcomes': [{'measure': 'Subject Self Reported Numerical Rating of Incidence and Severity of Post Electroconvulsive Therapy Headache After Treatment Day 1', 'timeFrame': '1 hour, 6 hours, 24 hours & 48 hours following procedure', 'description': 'Subject self reported numerical rating of incidence and severity of Post ECT pain score for headache at 1, 6, 24 and 48 hours post procedure. Pain Rating 0= no pain, 2-4=moderate pain, 5-7=distressing severe pain, 8-9=intense very severe pain, 10=unbearable pain'}, {'measure': 'Incidence and Severity of Headache After ECT Treatment 2', 'timeFrame': '1 hour, 6 hour, 24 hour and 48 hours', 'description': 'Subject self reported numerical rating of incidence and severity of post ECT headache 0=no pain, 2-4=moderate pain, 5-7= distressing severe pain, 8-9= very severe pain, 10=unbearable pain.'}, {'measure': 'Incidence of Headache & Severity Headache After ECT Treatment #3', 'timeFrame': '1 hour after treatment, 6 hours, 24 hours and 48 hours', 'description': 'Subject self reported numerical rating of incidence and severity of post ECT headache after treatment #3, 0=no pain, 2-4=moderate pain, 5-7=distressing severe pain, 8-9 very serious pain, 10=unbearable pain.'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'keywords': ['depression,myalgia'], 'conditions': ['Depression, Myalgia']}, 'descriptionModule': {'briefSummary': 'Post-procedure myalgia (muscle ache) is a well-known and common complication of Electro-convulsive Treatment (ECT). Myalgias are a serious concern of patients and occur in approximately 50% of these cases. The pain is usually described as muscle soreness, similar to that resulting from strenuous exercise. The myalgias typically begin shortly after the procedure, lasting approximately 2-7 days in total. A recent study reported that 89% of patients considered prevention significant and would be willing to pay a median of $33 out of pocket to avoid this side effect. In addition to patient discomfort, myalgias can have a further financial burden if these patients are unable to return to work or resume previous daily activities in the days following the procedure. An agent that could treat and possibly even prevent these myalgias has the potential to be very beneficial to these patients. IV ibuprofen (trade name Caldolor) is a novel therapeutic modality approved by the US Food and Drug Administration (FDA) in June 2009 for the treatment of mild to moderate pain, as an adjunct to opioid analgesics, and for the reduction of fever.', 'detailedDescription': "IV ibuprofen (trade name Caldolor) is a novel therapeutic modality approved by the US Food and Drug Administration (FDA) in June 2009 for the treatment of mild to moderate pain, as an adjunct to opioid analgesics, and for the reduction of fever. Ibuprofen is a non-steroidal anti-inflammatory drug (NSAID), which produces its effect through inhibition of the enzyme cyclooxygenase (COX). There are at least 2 variations of cyclooxygenase (COX-1 and COX-2) and ibuprofen non-selectively inhibits both, thus decreasing prostaglandin synthesis. This action gives ibuprofen its analgesic, anti-pyretic, and anti-inflammatory properties. NSAIDs have an established history of efficacy in the treatment of both acute and chronic somatic pain. Caldolor, being an intravenous formulation, offers a distinct advantage in patients who either are unable to take medications orally or are fasting preoperatively.\n\nPost-procedure myalgia is a well-known and common complication of ECT. Although the exact etiology is unknown, the myalgias are believed to result from a combination of succinylcholine administration and the seizure activity induced by the ECT procedure itself. Succinylcholine-induced postoperative myalgias are a well-known phenomenon, initially described in the early 1950's. The exact pathogenesis is unknown, with muscle damage from succinylcholine-induced fasciculations or calcium-mediated phospholipase A2 activation and prostaglandin production being proposed as possible etiologies. The latter mechanism provides the rationale for using NSAID therapy. However, succinylcholine is unlikely to be the only factor involved in the development of myalgias following ECT, as a recent study showed that dose adjustments to succinylcholine did not affect rates of myalgia in these patients. Furthermore, seizures can also cause direct muscle injury and there have been reports of muscle pain after ECT both with and without succinylcholine.\n\nA thorough literature search using Medline, Ovid, and scholar.google failed to find any research articles evaluating pretreatment therapy for myalgias in post-ECT patients. The current practice for the treatment of myalgias following ECT has been extrapolated from research on succinylcholine-induced myalgia in post-surgical patients. Previous studies have shown at least partial efficacy with pretreatment of nondepolarizing neuromuscular blocking agents, benzodiazepines, sodium channel blockers (predominantly lidocaine), and nonsteroidal anti-inflammatory drugs. The nature of the ECT procedure itself makes several of these modalities undesirable. Both Lidocaine and benzodiazepines can alter the seizure threshold and the short duration of the procedure possibly increases the risks associated with longer acting nondepolarizing muscle relaxants (ie. blurred vision, diplopia, difficulty breathing and swallowing). Therefore, the options for pretreatment are limited. In addition, a recent meta-analysis of randomized trials determined NSAIDs to cumulatively have the best efficacy of any pretreatment therapy in the prevention of post-procedural myalgias. Due to its intravenous formulation, some practitioners have administered ketorolac to ECT patients before the procedure. However, despite a proven efficacy in myalgia prevention shown by NSAIDs as a class, a study specifically examining the use of ketorolac in this regard failed to show any benefit. The use of Ibuprofen has yet to be examined.\n\nMyalgias are a serious concern of patients and occur in approximately 50% of these cases. The pain is usually described as muscle soreness, similar to that resulting from strenuous exercise. The myalgias typically begin shortly after the procedure, lasting approximately 2-7 days in total. A recent study reported that 89% of patients considered prevention significant and would be willing to pay a median of $33 out of pocket to avoid this side effect. In addition to patient discomfort, myalgias can have a further financial burden if these patients are unable to return to work or resume previous daily activities in the days following the procedure. An agent that could treat and possibly even prevent these myalgias has the potential to be very beneficial to these patients.\n\nExperimental Plan:\n\nThe study will be a prospective, randomized, double-blinded placebo-controlled clinical trial. The subject population will consist of patients undergoing first time electroconvulsive therapy, ranging in age from 18 to 80 years. Subjects will be given a Mini-Mental State Examination at the time of their presentation for ECT to assess their cognitive ability. If the patient consents and fits the inclusion criteria, patients will be randomized to one treatment modality, which they will receive for the first three treatment sessions. The subject and the person collecting the data will both be blinded as to what treatment modality the subject belongs to. The patients will be divided into two groups, Group 1 and Group 2. Group 1 will be treated with IV ibuprofen 800mg/8ml given over 30 minutes, prior to induction for ECT; while Group 2 will receive an identically appearing placebo dose, also administered IV, over that same time period. Both groups will receive a standardized anesthetic consisting of methohexital at 1 mg/kg IV for induction and succinylcholine 1 mg/kg IV for muscle paralysis. Other medications (eg. anticholinergic or antihypertensive drugs) will be administered at the discretion of the anesthesiologist. ECT will be administered by the psychiatrist in order to achieve a seizure with a motor component of \\> 15 second duration. Patients will be transported to the recovery room for post-anesthesia care. Rescue analgesics (Tylenol 500mg PO, Tylenol with codeine 300/30mg PO, Fentanyl 25 mcg IV) will be available to any patient with complaints of myalgia or headache pain of VAS \\>4.\n\nMeasurement Tools:\n\nSeverity of myalgias will be assessed based on a self-reported assessment utilizing a numerical rating scale (NRS). The scale will be rated as 0 meaning no pain at all and 10 meaning that pain is so severe as to interfere with daily activities.\n\nQuestionnaire:\n\nDo you have any muscle aches or pain right now? If yes, how would you rate that muscle ache/pain on a scale of 0 to 10, with 0 being no pain and 10 being pain that is the worst imaginable?\n\nExample:\n\n0 = No pain 1-3 = Mild Pain (nagging, annoying, little interference with everyday activities) 4-6 = Moderate Pain (interferes significantly with everyday activities) 7-10 = Severe Pain (unable to perform everyday activities) Have you had to take any medications to treat your muscle aches? If yes, what medication did you take? How many pills? What was the strength of the medication? Do you have a headache right now? If yes, how would you rate that headache on a scale of 0 to 10, with 0 being no pain and 10 being pain that is the worst imaginable?\n\nMeasurements:\n\nEach patient will have a self-reported numerical pain score assessed at baseline before therapy, 1 hour post-ECT, 6 hours post-ECT, 24 hours post-ECT, and finally at 48 hours post-ECT. The 6, 24 and 48 hour post-ECT assessments will be conducted via a telephone conversation. The use of rescue analgesics during recovery will also be documented as well as time from the end of procedure to discharge. The presence of headache will also be documented in each patient."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'maximumAge': '80 Years', 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Capable of providing informed consent\n* American Society Anesthesiologists (ASA) rating I-III\n* Subjects age 18-80 capable of providing consent.\n* Subjects undergoing electroconvulsive therapy using succinylcholine as the sole neuromuscular blocking agent.\n* Subjects who have scored ≥23 on the Mini-Mental State Examination.\n\nExclusion Criteria:\n\n* Subjects who have had a recent thrombotic event, myocardial infarction or stroke or episode of Congestive Heart Failure (CHF) within less than 3 months.\n* Subjects who have had a recent cardiovascular surgery within the last 3 months.\n* Subjects with active Gastrointestinal bleeding\n* Subjects who have asthma, itching or allergic type reaction following aspirin or other NSAID administration\n* Subjects with a known hypersensitivity to ibuprofen\n* Subjects with heart failure, bleeding disorders or kidney failure\n* Subjects taking aspirin, Angiotensin converting enzyme (ACE) inhibitors, or anticoagulants within one month.\n* Subjects with any devices used to treat pain (intrathecal pumps, spinal cord stimulators etc)\n* Subjects with a history of fibromyalgia or chronic myositis\n* Subjects who are pregnant\n* Subjects who do not have a phone\n* Subjects who have had previous ECT\n* Subjects receiving toradol (Ketorolac)\n* Subjects with reported renal disease within less than 3 months.\n* Subjects who have had previous electroconvulsive therapy within the last 3 months'}, 'identificationModule': {'nctId': 'NCT01200069', 'briefTitle': 'IV Ibuprofen for Post-Electroconvulsive Therapy Myalgia', 'organization': {'class': 'OTHER', 'fullName': 'Rutgers, The State University of New Jersey'}, 'officialTitle': 'Intravenous Ibuprofen/Caldolor for Post-Electroconvulsive Therapy Myalgia', 'orgStudyIdInfo': {'id': '0120100189'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'PLACEBO_COMPARATOR', 'label': 'Sugar water', 'description': '500 milliliters of intravenous ringers lactate administered over 30 minutes prior to ECT for treatments 1,2 and 3', 'interventionNames': ['Drug: Placebo infusion']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Ibuprofen', 'description': '300mg/8milliliters of intravenous ibuprofen/caldolor over 30 min in 500mL of ringers lactate to be administered prior to ECT for treatments # 1, 2 and 3', 'interventionNames': ['Drug: ibuprofen intravenous']}], 'interventions': [{'name': 'Placebo infusion', 'type': 'DRUG', 'otherNames': ['lactated ringers'], 'description': 'Identically appearing placebo dose administered IV prior to ECT and subsequently on ECT treatments 2 and 3', 'armGroupLabels': ['Sugar water']}, {'name': 'ibuprofen intravenous', 'type': 'DRUG', 'otherNames': ['Caldolor'], 'description': 'IV ibuprofen 800mg/8ml given over 30 minutes prior to ECT and subsequently on ECT treatments 2 and 3', 'armGroupLabels': ['Ibuprofen']}]}, 'contactsLocationsModule': {'locations': [{'zip': '07101', 'city': 'Newark', 'state': 'New Jersey', 'country': 'United States', 'facility': 'University Hospital', 'geoPoint': {'lat': 40.73566, 'lon': -74.17237}}], 'overallOfficials': [{'name': 'Vasanti Tilak, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'UMDNJ-NJMS'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Rutgers, The State University of New Jersey', 'class': 'OTHER'}, 'responsibleParty': {'type': 'SPONSOR'}}}}