Ignite Creation Date:
2025-12-24 @ 11:39 PM
Ignite Modification Date:
2025-12-25 @ 9:30 PM
Study NCT ID:
NCT01418651
Status:
TERMINATED
Last Update Posted:
2011-08-17
First Post:
2011-03-28
Is NOT Gene Therapy:
False
Has Adverse Events:
False
Brief Title:
Efficacy and Safety of Milnacipran in the Treatment of Fibromyalgia in an Elderly Population
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D005356', 'term': 'Fibromyalgia'}], 'ancestors': [{'id': 'D009135', 'term': 'Muscular Diseases'}, {'id': 'D009140', 'term': 'Musculoskeletal Diseases'}, {'id': 'D012216', 'term': 'Rheumatic Diseases'}, {'id': 'D009468', 'term': 'Neuromuscular Diseases'}, {'id': 'D009422', 'term': 'Nervous System Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D000078764', 'term': 'Milnacipran'}], 'ancestors': [{'id': 'D003521', 'term': 'Cyclopropanes'}, {'id': 'D003516', 'term': 'Cycloparaffins'}, {'id': 'D006840', 'term': 'Hydrocarbons, Alicyclic'}, {'id': 'D006844', 'term': 'Hydrocarbons, Cyclic'}, {'id': 'D006838', 'term': 'Hydrocarbons'}, {'id': 'D009930', 'term': 'Organic Chemicals'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 20}}, 'statusModule': {'whyStopped': 'Lack of subjects', 'overallStatus': 'TERMINATED', 'startDateStruct': {'date': '2011-03'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2011-01', 'completionDateStruct': {'date': '2011-08', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2011-08-16', 'studyFirstSubmitDate': '2011-03-28', 'studyFirstSubmitQcDate': '2011-08-16', 'lastUpdatePostDateStruct': {'date': '2011-08-17', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2011-08-17', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2011-08', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Change in self-reported severity of pain over 12 weeks of treatment in persons aged 65 and older', 'timeFrame': '14 months', 'description': 'Percent change in self-reported severity of pain (averaged Visual Analog Scale scores) over 12 weeks of treatment.\n\nRate of occurrence of adverse events necessitating drug discontinuation'}], 'secondaryOutcomes': [{'measure': 'Determine the effects of milnacipran on cognition', 'timeFrame': '14 months', 'description': 'Change in functional activity (FIQ), perceived health (SF-36), and severity of pain (Gracely scale).\n\nIncidence and severity of treatment-emergent adverse events. Change in sleep quality and daytime sleepiness as measured by the Pittsburgh Sleep Quality Index and Epworth Sleepiness Scale.\n\nChange in other sleep/wake parameters(actigraphy measures). Change in cognitive test scores from baseline to the 12 week visit. Patient global impression of change score.'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'conditions': ['Fibromyalgia']}, 'descriptionModule': {'briefSummary': 'Participants will undertake a 12-week, open-label study of milnacipran in a well-characterized cohort of patients with fibromyalgia syndrome (FMS) who are 65 years and older to investigate the short-term efficacy and safety of this drug in the elderly population. The investigators hypothesize that milnacipran will be effective in treating fibromyalgia syndrome (FMS), and will be prove to be safe when patients are selected for the absence of pre-existing blood pressure abnormalities and other serious medical conditions.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['OLDER_ADULT'], 'minimumAge': '65 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Male or female patients.\n* Age 65 years or older.\n* Fibromyalgia diagnosed according to ACR 1990 criteria.\n* Pain Score ≥ 10 on Gracely scale at screening and baseline assessments.\n* Discontinuation of other dual-acting antidepressant medications, including duloxetine, venlafaxine, and tricyclic antidepressants for a period not less than 4.5 times the drug half-life as of the baseline evaluation.\n\nExclusion Criteria:\n\n* Uncontrolled hypertension (BP ≥ 140/90) at screening or baseline evaluations.\n* Baseline orthostasis (documented drop in SBP ≥ 20 mmHg or in DBP ≥ 10 mmHg within 3 minutes after standing) at screening or baseline evaluations.\n* Psychosis, active suicidality, current episode of major depression or other severe psychiatric illness, or current alcohol/substance abuse or dependence as assessed by the MINI.\n* Significant cardiovascular disease, including atrial fibrillation or other dysrhythmia, congestive heart failure, valvular heart disease, or QTc prolongation on baseline EKG (\\> 450 msec).\n* Uncontrolled narrow angle glaucoma.\n* History of seizures.\n* Use of MAO inhibitor drugs within the last 14 days.\n* Abnormal baseline liver or renal function tests.\n* Dementia or other syndrome of cognitive impairment that could interfere with the subject's ability to participate fully in the assessment protocol.\n* Obstructive uropathy in males."}, 'identificationModule': {'nctId': 'NCT01418651', 'briefTitle': 'Efficacy and Safety of Milnacipran in the Treatment of Fibromyalgia in an Elderly Population', 'organization': {'class': 'OTHER', 'fullName': 'Banner Health'}, 'officialTitle': 'Efficacy and Safety of Milnacipran in the Treatment of Fibromyalgia in an Elderly Population: an Open-label Study', 'orgStudyIdInfo': {'id': '10-007'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Milnacipran', 'description': 'Drug', 'interventionNames': ['Drug: Savella']}], 'interventions': [{'name': 'Savella', 'type': 'DRUG', 'description': 'milnacipran 25 to 200 mg daily, divided into two doses (morning and evening)', 'armGroupLabels': ['Milnacipran']}]}, 'contactsLocationsModule': {'locations': [{'zip': '85351', 'city': 'Sun City', 'state': 'Arizona', 'country': 'United States', 'facility': 'Banner Sun Health Research Institute', 'geoPoint': {'lat': 33.59754, 'lon': -112.27182}}], 'overallOfficials': [{'name': 'Sandra Jacobson, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Banner Health'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Banner Health', 'class': 'OTHER'}, 'collaborators': [{'name': 'Forest Laboratories', 'class': 'INDUSTRY'}], 'responsibleParty': {'oldNameTitle': 'Sandra Jacobson MD - Research Physician', 'oldOrganization': 'Banner Sun Health Research Inst.'}}}}