{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Arch+cohort", "query": { "intervention": "Arch cohort" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 9, "total_pages": 1, "next_page_url": null, "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-07T20:26:17.310Z", "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.", "notes": [ "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.", "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.", "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees." ], "trials": [ { "nct_id": "NCT05800743", "title": "Evaluation of the GORE® Ascending Stent Graft", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Aortic Aneurysm, Thoracic", "Pseudoaneurysm", "Aortic Dissection", "Aorta; Lesion" ], "interventions": [ { "name": "GORE® Ascending Stent Graft (ASG device)", "type": "DEVICE" }, { "name": "GORE® Thoracic Aortic Graft Thoracic Branch Endoprosthesis (TBE Device)", "type": "DEVICE" }, { "name": "Surgery", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "W.L.Gore & Associates", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 370, "start_date": "2023-11-28", "completion_date": "2034-01", "has_results": false, "last_update_posted_date": "2026-05-29", "last_synced_at": "2026-09-07T20:26:17.310Z", "location_count": 41, "location_summary": "Birmingham, Alabama • Long Beach, California • Los Angeles, California + 37 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Long Beach", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Stanford", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05800743" }, { "nct_id": "NCT01740115", "title": "Boston Alcohol Research Collaboration on HIV/AIDS (ARCH) Cohort", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "HIV Infection", "Alcohol Use", "Bone Disease", "Substance-Related Disorders" ], "interventions": [], "intervention_types": [], "sponsor": "Boston Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 250, "start_date": "2012-11", "completion_date": "2016-08", "has_results": false, "last_update_posted_date": "2016-09-12", "last_synced_at": "2026-09-07T20:26:17.310Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01740115" }, { "nct_id": "NCT02777593", "title": "Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 2", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Aortic Aneurysm, Thoracic", "Aorta; Lesion" ], "interventions": [ { "name": "GORE® TAG® Thoracic Branch Endoprosthesis", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "W.L.Gore & Associates", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 250, "start_date": "2016-09-06", "completion_date": "2027-12", "has_results": true, "last_update_posted_date": "2026-03-09", "last_synced_at": "2026-09-07T20:26:17.310Z", "location_count": 35, "location_summary": "Los Angeles, California • Stanford, California • Hartford, Connecticut + 29 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Stanford", "state": "California" }, { "city": "Hartford", "state": "Connecticut" }, { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT02777593" }, { "nct_id": "NCT00455325", "title": "Chloroquine to Treat People With Metabolic Syndrome Aim2 (ARCH-MS)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Metabolic Syndrome X", "Overweight", "Hypertension", "Dyslipidemias", "Prediabetic State" ], "interventions": [ { "name": "Placebo Comparator: First Intervention (3 weeks)", "type": "DRUG" }, { "name": "Active Comparator: Second Intervention (3 weeks)", "type": "DRUG" }, { "name": "Active Comparator: Third Intervention (3 weeks)", "type": "DRUG" }, { "name": "Active Comparator: Fourth Intervention (3 weeks)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 35, "start_date": "2004-09", "completion_date": "2012-03", "has_results": true, "last_update_posted_date": "2022-05-10", "last_synced_at": "2026-09-07T20:26:17.310Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT00455325" }, { "nct_id": "NCT05639556", "title": "Strength and Muscle Related Outcomes for Nutrition and Lung Function in CF", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cystic Fibrosis" ], "interventions": [ { "name": "BMI and lean mass index from DXA", "type": "DIAGNOSTIC_TEST" }, { "name": "Anthropometric Measurements", "type": "DIAGNOSTIC_TEST" }, { "name": "Hand-grip strength", "type": "DIAGNOSTIC_TEST" }, { "name": "Six-minute walk Test", "type": "DIAGNOSTIC_TEST" }, { "name": "Sit-to-Stand Test", "type": "DIAGNOSTIC_TEST" }, { "name": "Short physical performance battery (SPPB)", "type": "DIAGNOSTIC_TEST" }, { "name": "BIA Sub-study", "type": "DIAGNOSTIC_TEST" }, { "name": "Accelerometry to assess physical activity", "type": "DIAGNOSTIC_TEST" }, { "name": "Gastrointestinal (GI) and nutrition questionnaires:", "type": "OTHER" }, { "name": "Psychosocial questionnaire: PHQ-8", "type": "OTHER" }, { "name": "Psychosocial questionnaire: GAD-7", "type": "OTHER" }, { "name": "Psychosocial questionnaire: The Treatment Self-Regulation Questionnaire (TSRQ)", "type": "OTHER" }, { "name": "Psychosocial questionnaire: CF Fatalism Scale", "type": "OTHER" }, { "name": "Psychosocial questionnaire: Body Esteem Scale for Adolescents and Adults (BESAA)", "type": "OTHER" }, { "name": "12-month Questionnaire", "type": "OTHER" }, { "name": "Oral glucose tolerance testing (OGTT)", "type": "OTHER" }, { "name": "Continuous glucose monitoring (CGM)", "type": "DEVICE" }, { "name": "Chest CT scans (When available within the past 6 months in medical records)", "type": "DIAGNOSTIC_TEST" }, { "name": "Hologic Dual X-Ray Absorptiometry (DXA)", "type": "DIAGNOSTIC_TEST" }, { "name": "Ultrasound Sub-study of assessment of appendage muscles using ultrasound", "type": "DIAGNOSTIC_TEST" }, { "name": "Psychosocial questionnaire: Hunger Vital Sign questionnaire", "type": "DIAGNOSTIC_TEST" }, { "name": "Respiratory symptom questionnaire: CRISS", "type": "OTHER" }, { "name": "Spirometry", "type": "DIAGNOSTIC_TEST" }, { "name": "Psychosocial questionnaire: Additional Health Questionnaire", "type": "OTHER" }, { "name": "CF Management Questionnaire", "type": "OTHER" }, { "name": "Food Frequency Questionnaire", "type": "OTHER" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "OTHER", "DEVICE" ], "sponsor": "Jaeb Center for Health Research", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 300, "start_date": "2023-04-20", "completion_date": "2028-12", "has_results": false, "last_update_posted_date": "2026-03-13", "last_synced_at": "2026-09-07T20:26:17.310Z", "location_count": 23, "location_summary": "Tucson, Arizona • Little Rock, Arkansas • Atlanta, Georgia + 19 more", "locations": [ { "city": "Tucson", "state": "Arizona" }, { "city": "Little Rock", "state": "Arkansas" }, { "city": "Atlanta", "state": "Georgia" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Iowa City", "state": "Iowa" } ], "official_url": "https://clinicaltrials.gov/study/NCT05639556" }, { "nct_id": "NCT01524211", "title": "Evaluation of Branch Endografts in the Treatment of Aortic Aneurysms", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Thoracoabdominal Aortic Aneurysm", "Aortic Arch Aneurysm" ], "interventions": [ { "name": "Zenith® t-Branch", "type": "DEVICE" }, { "name": "Terumo Arch Branch", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Baptist Health South Florida", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 235, "start_date": "2012-01-25", "completion_date": "2032-01", "has_results": false, "last_update_posted_date": "2026-06-15", "last_synced_at": "2026-09-07T20:26:17.310Z", "location_count": 1, "location_summary": "Boca Raton, Florida", "locations": [ { "city": "Boca Raton", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT01524211" }, { "nct_id": "NCT02266719", "title": "Clinical Outcomes and Radiation Safety After Endovascular Repair of Complex AAAs Using Fenestrated- Branched Devices", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Aortic Aneurysm, Abdominal", "Thoracic Aneurysm" ], "interventions": [ { "name": "Fenestrated CMD", "type": "DEVICE" }, { "name": "Type I - III TAAA", "type": "DEVICE" }, { "name": "Arch cohort", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Carlos Timaran", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 750, "start_date": "2014-12-01", "completion_date": "2028-12", "has_results": false, "last_update_posted_date": "2026-05-12", "last_synced_at": "2026-09-07T20:26:17.310Z", "location_count": 4, "location_summary": "Atlanta, Georgia • Dallas, Texas", "locations": [ { "city": "Atlanta", "state": "Georgia" }, { "city": "Atlanta", "state": "Georgia" }, { "city": "Atlanta", "state": "Georgia" }, { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT02266719" }, { "nct_id": "NCT03414411", "title": "Boston Alcohol Research Collaboration on HIV/AIDS (ARCH) Cohort: The 4F Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "HIV Infections", "Alcohol Drinking", "Substance-Related Disorders", "Bone Diseases", "Falls Injury", "Fractures, Bone", "Injuries" ], "interventions": [], "intervention_types": [], "sponsor": "Boston University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 251, "start_date": "2018-02-20", "completion_date": "2023-04-27", "has_results": false, "last_update_posted_date": "2023-06-07", "last_synced_at": "2026-09-07T20:26:17.310Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03414411" }, { "nct_id": "NCT03075865", "title": "A Cohort Study for Clinical Evaluation of OmniMax MMF System", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Mandibular Fractures" ], "interventions": [ { "name": "OmniMax MMF system", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Zimmer Biomet", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 39, "start_date": "2017-06-28", "completion_date": "2019-06-28", "has_results": false, "last_update_posted_date": "2021-07-19", "last_synced_at": "2026-09-07T20:26:17.310Z", "location_count": 3, "location_summary": "Sacramento, California • Iowa City, Iowa • Charleston, South Carolina", "locations": [ { "city": "Sacramento", "state": "California" }, { "city": "Iowa City", "state": "Iowa" }, { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03075865" } ] }