Ignite Creation Date:
2025-12-24 @ 4:00 PM
Ignite Modification Date:
2025-12-25 @ 3:51 PM
Study NCT ID:
NCT01515566
Status:
COMPLETED
Last Update Posted:
2014-08-22
First Post:
2012-01-13
Is NOT Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
Breakthrough Dyspnea Fentanyl Study in Cancer Patients
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D004417', 'term': 'Dyspnea'}], 'ancestors': [{'id': 'D012120', 'term': 'Respiration Disorders'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}, {'id': 'D012818', 'term': 'Signs and Symptoms, Respiratory'}, {'id': 'D012816', 'term': 'Signs and Symptoms'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D005283', 'term': 'Fentanyl'}, {'id': 'D011795', 'term': 'Surveys and Questionnaires'}], 'ancestors': [{'id': 'D010880', 'term': 'Piperidines'}, {'id': 'D006573', 'term': 'Heterocyclic Compounds, 1-Ring'}, {'id': 'D006571', 'term': 'Heterocyclic Compounds'}, {'id': 'D003625', 'term': 'Data Collection'}, {'id': 'D004812', 'term': 'Epidemiologic Methods'}, {'id': 'D008919', 'term': 'Investigative Techniques'}, {'id': 'D017531', 'term': 'Health Care Evaluation Mechanisms'}, {'id': 'D011787', 'term': 'Quality of Health Care'}, {'id': 'D017530', 'term': 'Health Care Quality, Access, and Evaluation'}, {'id': 'D011634', 'term': 'Public Health'}, {'id': 'D004778', 'term': 'Environment and Public Health'}]}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'CR_Study_Registration@mdanderson.org', 'phone': '713-792-6085', 'title': 'David Hui, MD, MSc, FRCPC / Asst. Professor, Palliative Care and Rehabilitation Medicine', 'organization': 'University of Texas MD Anderson Cancer Center'}, 'certainAgreement': {'piSponsorEmployee': True}, 'limitationsAndCaveats': {'description': 'The small sample size means findings are susceptible to random errors and regression to the mean.'}}, 'adverseEventsModule': {'timeFrame': 'Adverse effect collection from baseline up to 100 minutes for study participation.', 'eventGroups': [{'id': 'EG000', 'title': 'Fentanyl', 'description': 'Fentanyl SQ dose equivalent to 15-25% of the morphine equivalent daily dose (MEDD) 15 minutes before walk test. 6 minute walk test at baseline and 15 minutes after Fentanyl.', 'otherNumAtRisk': 10, 'otherNumAffected': 2, 'seriousNumAtRisk': 10, 'seriousNumAffected': 0}, {'id': 'EG001', 'title': 'Placebo', 'description': 'Normal saline 0.9% preservative free SQ 15 minutes before walk test. 6 minute walk test at baseline and 15 minutes after Placebo.', 'otherNumAtRisk': 10, 'otherNumAffected': 0, 'seriousNumAtRisk': 10, 'seriousNumAffected': 0}], 'otherEvents': [{'term': 'Pain with subcutaneous injection', 'stats': [{'groupId': 'EG000', 'numAtRisk': 10, 'numEvents': 2, 'numAffected': 2}, {'groupId': 'EG001', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}], 'organSystem': 'General disorders', 'assessmentType': 'NON_SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'SNOMED CT'}], 'frequencyThreshold': '5'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'SECONDARY', 'title': 'Effect of Fentanyl Versus Placebo for Exercise-Induced and Breakthrough Dyspnea', 'denoms': [{'units': 'Participants', 'counts': [{'value': '10', 'groupId': 'OG000'}, {'value': '10', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Fentanyl', 'description': 'Fentanyl SQ dose equivalent to 15-25% of MEDD 15 minutes before walk test; 6MWT at baseline and 15 minutes after Fentanyl.'}, {'id': 'OG001', 'title': 'Placebo', 'description': 'Normal saline 0.9% preservative free SQ 15 minutes before walk test; 6MWT at baseline and 15 minutes after Placebo.'}], 'classes': [{'title': 'Dyspnea at 0 minutes (Baseline walk test)', 'categories': [{'measurements': [{'value': '2', 'spread': '1', 'groupId': 'OG000', 'lowerLimit': '1.8', 'upperLimit': '.4'}, {'value': '3', 'spread': '3', 'groupId': 'OG001', 'lowerLimit': '1.5', 'upperLimit': '.1'}]}]}, {'title': 'Dyspnea at 6 minutes (Baseline walk test)', 'categories': [{'measurements': [{'value': '6', 'spread': '1', 'groupId': 'OG000', 'lowerLimit': '3.2', 'upperLimit': '.4'}, {'value': '7', 'spread': '3', 'groupId': 'OG001', 'lowerLimit': '4', 'upperLimit': '.02'}]}]}, {'title': 'Dyspnea at 0 minutes (Second walk test)', 'categories': [{'measurements': [{'value': '1', 'spread': '1', 'groupId': 'OG000', 'lowerLimit': '1.8', 'upperLimit': '.04'}, {'value': '2', 'spread': '2', 'groupId': 'OG001', 'lowerLimit': '1.5', 'upperLimit': '.1'}]}]}, {'title': 'Dyspnea at 6 minutes (Second walk test)', 'categories': [{'measurements': [{'value': '4', 'spread': '1', 'groupId': 'OG000', 'lowerLimit': '3.2', 'upperLimit': '.4'}, {'value': '5', 'spread': '3', 'groupId': 'OG001', 'lowerLimit': '4', 'upperLimit': '.02'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline to 100 minutes for study participation.', 'description': 'Participants receive either Fentanyl subcutaneous (SQ) 15 minutes before walking test, or Placebo (SQ) 15 minutes before walking test. During the study, trained research staff perform study assessments and monitor participant carefully throughout the study period. Six-minute walk tests were carried out following guidelines from the American Thoracic Society. The intensity of dyspnea at 0, 1, 2, 3, 4, 5 and 6 minute of each walk test were assessed using a validated numeric rating scale (NRS) ranging from 0 ("no shortness of breath") to 10 ("worst possible shortness of breath") and every 5 minutes during the rest period.', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED'}, {'type': 'PRIMARY', 'title': 'Retention Rate', 'denoms': [{'units': 'Participants', 'counts': [{'value': '10', 'groupId': 'OG000'}, {'value': '10', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Fentanyl', 'description': 'Fentanyl SQ dose equivalent to 15-25% of MEDD 15 minutes before walk test; 6MWT at baseline and 15 minutes after Fentanyl.'}, {'id': 'OG001', 'title': 'Placebo', 'description': 'Normal saline 0.9% preservative free SQ 15 minutes before walk test; 6MWT at baseline and 15 minutes after Placebo.'}], 'classes': [{'categories': [{'measurements': [{'value': '100', 'groupId': 'OG000'}, {'value': '100', 'groupId': 'OG001'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Baseline to study completion, up to 100 minutes.', 'description': 'Retention rate is defined as the percentage of subjects able to complete the study.', 'unitOfMeasure': 'percentage of participants', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Effect of Fentanyl on Walk Distance', 'denoms': [{'units': 'Participants', 'counts': [{'value': '10', 'groupId': 'OG000'}, {'value': '10', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Fentanyl', 'description': 'Fentanyl SQ dose equivalent to 15-25% of MEDD 15 minutes before walk test; 6MWT at baseline and 15 minutes after Fentanyl.'}, {'id': 'OG001', 'title': 'Placebo', 'description': 'Normal saline 0.9% preservative free SQ 15 minutes before walk test; 6MWT at baseline and 15 minutes after Placebo.'}], 'classes': [{'title': 'Walk Distance (Baseline Walk Test)', 'categories': [{'measurements': [{'value': '397.7', 'spread': '98.1', 'groupId': 'OG000'}, {'value': '399', 'spread': '86.4', 'groupId': 'OG001'}]}]}, {'title': 'Walk Distance (Second Walk Test)', 'categories': [{'measurements': [{'value': '434.9', 'spread': '95.4', 'groupId': 'OG000'}, {'value': '417.9', 'spread': '89.3', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': 'Baseline 6 minute walk test (6MWT) to second 6MWT, up to 100 minutes for study participation.', 'description': 'Ambulatory patients with breakthrough dyspnea performed a baseline 6 minute walk test (6MWT), and then received either subcutaneous fentanyl or placebo 15 minutes before a second 6MWT. The change in walk distance was documented between the first and second 6MWT.', 'unitOfMeasure': 'feet', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED'}]}, 'participantFlowModule': {'groups': [{'id': 'FG000', 'title': 'Fentanyl', 'description': 'Fentanyl subcutaneous (SQ) dose equivalent to 15-25% of the morphine equivalent daily dose (MEDD) 15 minutes before walk test; 6 minute walk test (6MWT) at baseline and 15 minutes after Fentanyl. Questionnaires completed at baseline and after study visit.'}, {'id': 'FG001', 'title': 'Placebo', 'description': 'Normal saline 0.9% preservative free SQ 15 minutes before walk test; 6 minute walk test (6MWT) at baseline and 15 minutes after Placebo. Questionnaires completed at baseline and after study visit.'}], 'periods': [{'title': 'Overall Study', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '10'}, {'groupId': 'FG001', 'numSubjects': '10'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '10'}, {'groupId': 'FG001', 'numSubjects': '10'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '0'}]}]}], 'recruitmentDetails': 'Outpatient participants from the Supportive Care Center at MD Anderson Cancer Center were recruited between July 10, 2012 and December 12, 2012.', 'preAssignmentDetails': 'Six participants of the 26 recruited were excluded from the trial before assignment to groups due to ineligibility.'}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '10', 'groupId': 'BG000'}, {'value': '10', 'groupId': 'BG001'}, {'value': '20', 'groupId': 'BG002'}]}], 'groups': [{'id': 'BG000', 'title': 'Fentanyl', 'description': 'Fentanyl SQ dose equivalent to 15-25% of the morphine equivalent daily dose (MEDD) 15 minutes before walk test; 6 minute walk test (6MWT) at baseline and 15 minutes after Fentanyl or Placebo. Questionnaires completed at baseline and after study visit.'}, {'id': 'BG001', 'title': 'Placebo', 'description': 'Normal saline 0.9% preservative free SQ 15 minutes before walk test; 6MWT at baseline and 15 minutes after Fentanyl or Placebo. Questionnaires completed at baseline and after study visit.'}, {'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': '7', 'groupId': 'BG000'}, {'value': '8', 'groupId': 'BG001'}, {'value': '15', 'groupId': 'BG002'}]}, {'title': '>=65 years', 'measurements': [{'value': '3', 'groupId': 'BG000'}, {'value': '2', 'groupId': 'BG001'}, {'value': '5', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '6', 'groupId': 'BG000'}, {'value': '5', 'groupId': 'BG001'}, {'value': '11', 'groupId': 'BG002'}]}, {'title': 'Male', 'measurements': [{'value': '4', 'groupId': 'BG000'}, {'value': '5', 'groupId': 'BG001'}, {'value': '9', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Region of Enrollment', 'classes': [{'title': 'United States', 'categories': [{'measurements': [{'value': '10', 'groupId': 'BG000'}, {'value': '10', 'groupId': 'BG001'}, {'value': '20', 'groupId': 'BG002'}]}]}], 'paramType': 'NUMBER', 'unitOfMeasure': 'participants'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1', 'PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'DOUBLE', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR']}, 'primaryPurpose': 'SUPPORTIVE_CARE', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 26}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2012-04'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2014-08', 'completionDateStruct': {'date': '2013-04', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2014-08-07', 'studyFirstSubmitDate': '2012-01-13', 'resultsFirstSubmitDate': '2014-08-07', 'studyFirstSubmitQcDate': '2012-01-18', 'lastUpdatePostDateStruct': {'date': '2014-08-22', 'type': 'ESTIMATED'}, 'resultsFirstSubmitQcDate': '2014-08-07', 'studyFirstPostDateStruct': {'date': '2012-01-24', 'type': 'ESTIMATED'}, 'resultsFirstPostDateStruct': {'date': '2014-08-22', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2013-04', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Retention Rate', 'timeFrame': 'Baseline to study completion, up to 100 minutes.', 'description': 'Retention rate is defined as the percentage of subjects able to complete the study.'}], 'secondaryOutcomes': [{'measure': 'Effect of Fentanyl Versus Placebo for Exercise-Induced and Breakthrough Dyspnea', 'timeFrame': 'Baseline to 100 minutes for study participation.', 'description': 'Participants receive either Fentanyl subcutaneous (SQ) 15 minutes before walking test, or Placebo (SQ) 15 minutes before walking test. During the study, trained research staff perform study assessments and monitor participant carefully throughout the study period. Six-minute walk tests were carried out following guidelines from the American Thoracic Society. The intensity of dyspnea at 0, 1, 2, 3, 4, 5 and 6 minute of each walk test were assessed using a validated numeric rating scale (NRS) ranging from 0 ("no shortness of breath") to 10 ("worst possible shortness of breath") and every 5 minutes during the rest period.'}, {'measure': 'Effect of Fentanyl on Walk Distance', 'timeFrame': 'Baseline 6 minute walk test (6MWT) to second 6MWT, up to 100 minutes for study participation.', 'description': 'Ambulatory patients with breakthrough dyspnea performed a baseline 6 minute walk test (6MWT), and then received either subcutaneous fentanyl or placebo 15 minutes before a second 6MWT. The change in walk distance was documented between the first and second 6MWT.'}]}, 'oversightModule': {'oversightHasDmc': True}, 'conditionsModule': {'keywords': ['Advanced Cancer', 'Dyspnea', 'Exercise-induced breakthrough dyspnea', 'Shortness of breath', 'Fentanyl', 'Sublimaze', 'Placebo', 'Normal saline', 'NS', 'Questionnaires', 'Surveys', 'Walk test'], 'conditions': ['Advanced Cancers', 'Dyspnea']}, 'referencesModule': {'references': [{'pmid': '23830530', 'type': 'DERIVED', 'citation': 'Hui D, Xu A, Frisbee-Hume S, Chisholm G, Morgado M, Reddy S, Bruera E. Effects of prophylactic subcutaneous fentanyl on exercise-induced breakthrough dyspnea in cancer patients: a preliminary double-blind, randomized, controlled trial. J Pain Symptom Manage. 2014 Feb;47(2):209-17. doi: 10.1016/j.jpainsymman.2013.03.017. Epub 2013 Jul 3.'}], 'seeAlsoLinks': [{'url': 'http://www.mdanderson.org', 'label': 'UT MD Anderson Cancer Center Website'}]}, 'descriptionModule': {'briefSummary': 'The goal of this clinical research study is to learn if fentanyl given under the skin can reduce shortness of breath in cancer patients. Researchers also want to learn if it can help to improve your physical function. In this study, fentanyl will be compared to a placebo.\n\nFentanyl is commonly used for treatment of cancer pain. It is believed to help patients with their shortness of breath as well.\n\nA placebo is not a drug. It looks like the study drug but is not designed to treat any disease or illness. It is designed to be compared with a study drug to learn if the study drug has any real effect.', 'detailedDescription': "Study Groups:\n\nIf you are found to be eligible to take part in this study, you will be randomly assigned (as in the flip of a coin) to either receive fentanyl or placebo. You will have an equal chance of being assigned to either group.\n\nStudy Drug/Placebo Administration:\n\nBefore you receive the study drug/placebo, you will walk back and forth in an indoor corridor for up to 6 minutes. You may feel out of breath or become exhausted. You may slow down, stop, and rest at any time you need to.\n\nAfter that, you will sit down and rest (for up to 1 hour). During this time, the study drug/placebo will be prepared.\n\nYou will then be given a study drug/placebo shot under the skin in your arms or legs. You will then wait for another 15 minutes and repeat the walking test.\n\nStudy Visit:\n\nDuring your study visit, the study staff will collect information from your medical record about your age, sex, race, disease type, how well you are able to perform the normal activities of daily living, any drugs you are taking, and possible causes of shortness of breath.\n\nYou will also complete 2 walking tests. Before the walk tests, you will complete 2 questionnaires. One (1) of them asks about any breathing symptoms you may be having, and the other asks about any other symptoms you may be having. It should take about 10 minutes to complete these questionnaires.\n\nBefore and after each walk test, the study staff will record your heart rate, breathing rate, and the level of air breathed out using a measuring device that will be clipped onto your finger. The study staff will also ask you questions about how hard it is to catch your breath and your level of tiredness.\n\nDuring each walk test, you will be asked about how hard it is to catch your breath. The distance you walked and how often and for how long you stopped will be recorded. Before and after the second walk test, the study staff will ask you about any side effects from the study drug/placebo that you may be having.\n\nDuring the rest period between the 2 walk tests, you may be asked how hard it is to catch your breath several times.\n\nAt the end of the study visit, you will fill out 1 questionnaire that asks if you think the study drug/placebo is helping you, and how satisfied you are with the study. It should take about 5 minutes to complete the questionnaire.\n\nLength of Study:\n\nYou will be on this study for up to 100 minutes.You will be taken off study if intolerable side effects occur during the study.\n\nThis is an investigational study. Fentanyl is FDA approved and commercially available for the treatment of pain. It's use to help with shortness of breath is investigational.\n\nUp to 20 patients will be enrolled in this study. All will be enrolled at MD Anderson."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n1. Diagnosis of cancer\n2. Breakthrough dyspnea, defined in this study as dyspnea on exertion with an average intensity level \\>=3/10 on the numeric rating scale\n3. Outpatient or inpatient at MD Anderson Cancer Center seen by the Supportive Care or Rehabilitation Service\n4. Able to communicate in English or Spanish\n5. Ambulatory and able to walk with or without walking aid\n6. On strong opioids with morphine equivalent daily dose of 30-580 mg, with stable (i.e. +/- 30%) regular dose over the last 24 hours\n7. Karnofsky performance status \\>=50%\n8. Age 18 or older\n\nExclusion Criteria:\n\n1. Dyspnea at rest \\>=7/10 at the time of enrollment\n2. Supplemental oxygen requirement \\>6 L per minute\n3. Delirium (i.e. Memorial delirium rating scale \\>13)\n4. History of unstable angina or myocardial infarction 1 month prior to study enrollment\n5. Resting heart rate \\>120 at the time of study enrollment\n6. Systolic pressure \\>180 mmHg or diastolic pressure \\>100 mmHg at the time of study enrollment\n7. History of active substance abuse within the past 12 months\n8. History of allergy to fentanyl\n9. Unwilling to provide informed consent'}, 'identificationModule': {'nctId': 'NCT01515566', 'briefTitle': 'Breakthrough Dyspnea Fentanyl Study in Cancer Patients', 'organization': {'class': 'OTHER', 'fullName': 'M.D. Anderson Cancer Center'}, 'officialTitle': 'Effects of Prophylactic Subcutaneous Fentanyl on Exercise-Induced Breakthrough Dyspnea in Cancer Patients: A Preliminary Double-Blind, Randomized Controlled Trial', 'orgStudyIdInfo': {'id': '2011-1007'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Fentanyl', 'description': 'Fentanyl subcutaneously (SQ) dose equivalent to 15-25% of the morphine equivalent daily dose (MEDD) 15 minutes before walk test, and 6 minute walk test (6MWT) at baseline and 15 minutes after Fentanyl. Two (2) Questionnaires completed at baseline taking about 10 minutes to complete, and one completed after study visit taking about 5 minutes to complete.', 'interventionNames': ['Drug: Fentanyl', 'Other: Walking Tests', 'Behavioral: Questionnaires']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Placebo', 'description': 'Normal saline 0.9% preservative free SQ 15 minutes before walk test, and 6 minute walk test at baseline and 15 minutes after Placebo. Two (2) Questionnaires completed at baseline taking about 10 minutes to complete, and one completed after study visit taking about 5 minutes to complete.', 'interventionNames': ['Other: Placebo', 'Other: Walking Tests', 'Behavioral: Questionnaires']}], 'interventions': [{'name': 'Fentanyl', 'type': 'DRUG', 'otherNames': ['Sublimaze'], 'description': 'Fentanyl SQ dose equivalent to 15-25% of the morphine equivalent daily dose (MEDD) 15 minutes before 6 minute walk test.', 'armGroupLabels': ['Fentanyl']}, {'name': 'Placebo', 'type': 'OTHER', 'description': 'Normal saline 0.9% preservative free SQ 15 minutes before walk test.', 'armGroupLabels': ['Placebo']}, {'name': 'Walking Tests', 'type': 'OTHER', 'description': '6 minute walk test at baseline and 15 minutes after Fentanyl or Placebo.', 'armGroupLabels': ['Fentanyl', 'Placebo']}, {'name': 'Questionnaires', 'type': 'BEHAVIORAL', 'otherNames': ['Surveys'], 'description': 'Questionnaires completed at baseline (two) and after study visit (one) taking about 5 ot 10 minutes to complete.', 'armGroupLabels': ['Fentanyl', 'Placebo']}]}, 'contactsLocationsModule': {'locations': [{'zip': '77030', 'city': 'Houston', 'state': 'Texas', 'country': 'United States', 'facility': 'UT MD Anderson Cancer Center', 'geoPoint': {'lat': 29.76328, 'lon': -95.36327}}], 'overallOfficials': [{'name': 'David Hui, MD', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'UT MD Anderson Cancer Center'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'M.D. Anderson Cancer Center', 'class': 'OTHER'}, 'responsibleParty': {'type': 'SPONSOR'}}}}