Ignite Creation Date:
2025-12-24 @ 9:14 PM
Ignite Modification Date:
2026-02-02 @ 1:48 AM
Study NCT ID:
NCT02873104
Status:
COMPLETED
Last Update Posted:
2018-02-28
First Post:
2016-08-16
Is NOT Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
Pivotal Study of the truSculpt Radiofrequency Device for Circumferential Reduction
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'lmoldre@cutera.com', 'phone': '415-971-5118', 'title': 'Lourdes Moldre, NP', 'organization': 'Cutera'}, 'certainAgreement': {'piSponsorEmployee': True}}, 'adverseEventsModule': {'eventGroups': [{'id': 'EG000', 'title': 'Treatment', 'description': 'truSculpt rf device, therapeutic settings\n\ntruSculpt rf device: radiofrequency device', 'otherNumAtRisk': 47, 'otherNumAffected': 47, 'seriousNumAtRisk': 47, 'seriousNumAffected': 0}, {'id': 'EG001', 'title': 'Sham', 'description': 'truSculpt rf device, non-therapeutic settings\n\ntruSculpt rf device: radiofrequency device', 'otherNumAtRisk': 23, 'otherNumAffected': 23, 'seriousNumAtRisk': 23, 'seriousNumAffected': 0}], 'otherEvents': [{'term': 'Erythema', 'stats': [{'groupId': 'EG000', 'numAtRisk': 47, 'numEvents': 47, 'numAffected': 47}, {'groupId': 'EG001', 'numAtRisk': 23, 'numEvents': 23, 'numAffected': 23}], 'organSystem': 'Skin and subcutaneous tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Edema', 'stats': [{'groupId': 'EG000', 'numAtRisk': 47, 'numEvents': 47, 'numAffected': 47}, {'groupId': 'EG001', 'numAtRisk': 23, 'numEvents': 0, 'numAffected': 0}], 'organSystem': 'Skin and subcutaneous tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}], 'frequencyThreshold': '1'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'PRIMARY', 'title': 'Difference in Circumferential Measurement Related to Sham and Therapeutic Group at 12 Weeks Post-treatment', 'denoms': [{'units': 'Participants', 'counts': [{'value': '46', 'groupId': 'OG000'}, {'value': '23', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment', 'description': 'truSculpt rf device, therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}, {'id': 'OG001', 'title': 'Sham', 'description': 'truSculpt rf device, non-therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}], 'classes': [{'categories': [{'measurements': [{'value': '1.9', 'spread': '0.1', 'groupId': 'OG000'}, {'value': '0', 'spread': '0.1', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '12 weeks', 'description': 'Change in Abdominal Circumferential Measurement Related to Sham and Therapeutic Group at 12 Weeks Post-treatment minus Baseline Measurement', 'unitOfMeasure': 'cm', 'dispersionType': 'Standard Error', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Subject Assessment of Improvement for Both Sham Group and Therapeutic Group at 12 Weeks Post-treatment.', 'denoms': [{'units': 'Participants', 'counts': [{'value': '46', 'groupId': 'OG000'}, {'value': '23', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment', 'description': 'truSculpt rf device, therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}, {'id': 'OG001', 'title': 'Sham', 'description': 'truSculpt rf device, non-therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}], 'classes': [{'categories': [{'measurements': [{'value': '2.4', 'spread': '1', 'groupId': 'OG000'}, {'value': '1', 'spread': '1.5', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '12 weeks', 'description': 'Comparison of the average subject improvement score for the sham group and the therapeutic group at 12 weeks post-treatment using a 0 - 4 improvement scale where 0 equals "no change" and 4 equals "Very Significant Improvement".', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Subject Satisfaction Level for Both Sham Group and Therapeutic Group at 12 Weeks Post-treatment.', 'denoms': [{'units': 'Participants', 'counts': [{'value': '46', 'groupId': 'OG000'}, {'value': '23', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment', 'description': 'truSculpt rf device, therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}, {'id': 'OG001', 'title': 'Sham', 'description': 'truSculpt rf device, non-therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}], 'classes': [{'categories': [{'measurements': [{'value': '4.1', 'spread': '0.8', 'groupId': 'OG000'}, {'value': '3.3', 'spread': '0.9', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '12 weeks', 'description': 'Comparison of the average subject satisfaction level for the sham group and therapeutic group at 12 weeks post-treatment, using a 1 - 5 scale where 1 equals "very dissatisfied" and 5 equals "very satisfied".', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Subject Discomfort and Pain Levels During Treatment', 'denoms': [{'units': 'Participants', 'counts': [{'value': '47', 'groupId': 'OG000'}, {'value': '23', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment', 'description': 'truSculpt rf device, therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}, {'id': 'OG001', 'title': 'Sham', 'description': 'truSculpt rf device, non-therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}], 'classes': [{'categories': [{'measurements': [{'value': '5.75', 'spread': '0.9', 'groupId': 'OG000'}, {'value': '1.1', 'spread': '0.3', 'groupId': 'OG001'}]}]}], 'paramType': 'MEAN', 'timeFrame': '12 weeks', 'description': 'Comparison of the average pain levels during treatment for the sham group and therapeutic group at 12 weeks post-treatment, using a 0 - 10 scale where 0 equals "No pain" and 10 equals "Worst possible pain".', 'unitOfMeasure': 'units on a scale', 'dispersionType': 'Standard Deviation', 'reportingStatus': 'POSTED'}]}, 'participantFlowModule': {'groups': [{'id': 'FG000', 'title': 'Treatment', 'description': 'truSculpt rf device, therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}, {'id': 'FG001', 'title': 'Sham', 'description': 'truSculpt rf device, non-therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}], 'periods': [{'title': 'Overall Study', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '47'}, {'groupId': 'FG001', 'numSubjects': '23'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '46'}, {'groupId': 'FG001', 'numSubjects': '23'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '1'}, {'groupId': 'FG001', 'numSubjects': '0'}]}]}]}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '47', 'groupId': 'BG000'}, {'value': '23', 'groupId': 'BG001'}, {'value': '70', 'groupId': 'BG002'}]}], 'groups': [{'id': 'BG000', 'title': 'Treatment', 'description': 'truSculpt rf device, therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}, {'id': 'BG001', 'title': 'Sham', 'description': 'truSculpt rf device, non-therapeutic settings\n\ntruSculpt rf device: radiofrequency device'}, {'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': '47', 'groupId': 'BG000'}, {'value': '23', 'groupId': 'BG001'}, {'value': '70', 'groupId': 'BG002'}]}, {'title': '>=65 years', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '37', 'groupId': 'BG000'}, {'value': '8', 'groupId': 'BG001'}, {'value': '45', 'groupId': 'BG002'}]}, {'title': 'Male', 'measurements': [{'value': '10', 'groupId': 'BG000'}, {'value': '15', 'groupId': 'BG001'}, {'value': '25', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}]}}, 'protocolSection': {'designModule': {'phases': ['NA'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'SINGLE', 'whoMasked': ['PARTICIPANT']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 70}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2016-03'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2017-02', 'completionDateStruct': {'date': '2016-09', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2018-01-31', 'studyFirstSubmitDate': '2016-08-16', 'resultsFirstSubmitDate': '2016-12-13', 'studyFirstSubmitQcDate': '2016-08-16', 'lastUpdatePostDateStruct': {'date': '2018-02-28', 'type': 'ACTUAL'}, 'resultsFirstSubmitQcDate': '2018-01-31', 'studyFirstPostDateStruct': {'date': '2016-08-19', 'type': 'ESTIMATED'}, 'resultsFirstPostDateStruct': {'date': '2018-02-28', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2016-09', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Difference in Circumferential Measurement Related to Sham and Therapeutic Group at 12 Weeks Post-treatment', 'timeFrame': '12 weeks', 'description': 'Change in Abdominal Circumferential Measurement Related to Sham and Therapeutic Group at 12 Weeks Post-treatment minus Baseline Measurement'}], 'secondaryOutcomes': [{'measure': 'Subject Assessment of Improvement for Both Sham Group and Therapeutic Group at 12 Weeks Post-treatment.', 'timeFrame': '12 weeks', 'description': 'Comparison of the average subject improvement score for the sham group and the therapeutic group at 12 weeks post-treatment using a 0 - 4 improvement scale where 0 equals "no change" and 4 equals "Very Significant Improvement".'}, {'measure': 'Subject Satisfaction Level for Both Sham Group and Therapeutic Group at 12 Weeks Post-treatment.', 'timeFrame': '12 weeks', 'description': 'Comparison of the average subject satisfaction level for the sham group and therapeutic group at 12 weeks post-treatment, using a 1 - 5 scale where 1 equals "very dissatisfied" and 5 equals "very satisfied".'}, {'measure': 'Subject Discomfort and Pain Levels During Treatment', 'timeFrame': '12 weeks', 'description': 'Comparison of the average pain levels during treatment for the sham group and therapeutic group at 12 weeks post-treatment, using a 0 - 10 scale where 0 equals "No pain" and 10 equals "Worst possible pain".'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDevice': True}, 'conditionsModule': {'conditions': ['Abdominal Fat']}, 'descriptionModule': {'briefSummary': 'To evaluate the safety and efficacy of the Cutera truSculpt radiofrequency device for circumferential reduction.', 'detailedDescription': 'The objectives of this study are to evaluate efficacy and safety of treatment with the Cutera truSculpt RF device for circumferential reduction in the abdominal and flank region.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT'], 'maximumAge': '60 Years', 'minimumAge': '24 Years', 'healthyVolunteers': True, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Female or Male, 24 to 60 years of age (inclusive). Fitzpatrick Skin Type I - VI. Has visible fat bulges on the abdomen and palpable fat pockets superior to iliac crest located bilaterally in the lower back flank region Has a Body Mass Index (BMI) ≥ 20 and ≤ 30 Non-smoking for at least 6 months and willing to refrain from smoking for the duration of the study.\n\nSubject must agree to not undergo any other procedure(s) in the abdominal and flank region during the study period.\n\nSubject must be able to read, understand and sign the Informed Consent Form. Subject must adhere to the follow-up schedule and study instructions. Subject must adhere to the same diet and/or exercise routine throughout the study, and agree to maintain the same weight throughout the study, within 5% of baseline weight measurement.\n\nWilling to have digital photographs taken of the treatment area and agree to use of photographs for presentation, educational or marketing purposes.\n\nPost-menopausal or surgically sterilized, or using a medically acceptable form of birth control at least 3 months prior to enrollment and during the entire course of the study, and no plans to become pregnant.\n\nExclusion Criteria:\n\n* Participation in a clinical trial of another device or drug within 6 months of study participation, or during the study period.\n\nAny type of prior cosmetic treatment to the target area within 12 months of study participation e.g., radiofrequency, cryolysis or light-based treatments.\n\nAny prior invasive cosmetic surgery to the target area, such as liposuction. Currently taking medications or supplements for weight-loss or metabolism support/enhancement or has a history of taking such medications or supplements within 3 months.\n\nHas a pacemaker, internal defibrillator, implantable cardioverter-defibrillator, nerve stimulator implant, cochlear implant or any other electronically, magnetically or mechanically activated implant.\n\nHas metal implant(s) within the body, such as surgical clips, plates and screws, intrauterine device (IUD), artificial heart valves or artificial joints.\n\nSignificant concurrent illness, such as diabetes mellitus, cardiovascular disease, peripheral vascular disease or pertinent neurological disorders.\n\nDiagnosed or documented immune system disorders. History of any disease or condition that could impair wound healing. History of diseases stimulated by heat, such as recurrent herpes zoster in the treatment area, unless treatment is conducted following a prophylactic regimen.\n\nHistory of keloid formation, hypertrophic scarring or abnormal/delayed wound healing.\n\nInfection, dermatitis, rash or other skin abnormality in the target area. Currently undergoing systemic chemotherapy or radiation treatment for cancer, or history of treatment in the target area within 3 months of study participation.\n\nPregnant or currently breastfeeding. As per the Investigator's discretion, any physical or mental condition which might make it unsafe for the subject to participate in this study."}, 'identificationModule': {'nctId': 'NCT02873104', 'briefTitle': 'Pivotal Study of the truSculpt Radiofrequency Device for Circumferential Reduction', 'organization': {'class': 'INDUSTRY', 'fullName': 'Cutera Inc.'}, 'officialTitle': 'Pivotal Study of the truSculpt Radiofrequency Device for Circumferential Reduction', 'orgStudyIdInfo': {'id': 'C-16-TS11'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'ACTIVE_COMPARATOR', 'label': 'Treatment', 'description': 'truSculpt rf device, therapeutic settings', 'interventionNames': ['Device: truSculpt rf device']}, {'type': 'SHAM_COMPARATOR', 'label': 'Sham', 'description': 'truSculpt rf device, non-therapeutic settings', 'interventionNames': ['Device: truSculpt rf device']}], 'interventions': [{'name': 'truSculpt rf device', 'type': 'DEVICE', 'description': 'radiofrequency device', 'armGroupLabels': ['Sham', 'Treatment']}]}, 'contactsLocationsModule': {'locations': [{'zip': '94005', 'city': 'Brisbane', 'state': 'California', 'country': 'United States', 'facility': 'Cutera Research Center', 'geoPoint': {'lat': 37.68077, 'lon': -122.39997}}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Cutera Inc.', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}