{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Implanted+Device&page=50", "query": { "intervention": "Implanted Device", "page": 50 }, "page_size": 10 }, "pagination": { "page": 50, "page_size": 10, "total_count": 1807, "total_pages": 181, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Implanted+Device&page=51&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Implanted+Device&page=49&page_size=10" }, "source": "remote", "last_synced_at": "2026-11-15T08:00:19.779Z", "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": "NCT04922281", "title": "Insertable Cardiac Monitor-Guided Early Intervention to Reduce Atrial Fibrillation Burden Following Catheter Ablation", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Atrial Fibrillation", "Cardiovascular Diseases", "Heart Diseases", "Arrhythmias, Cardiac", "Pathologic Processes" ], "interventions": [ { "name": "Insertable Cardiac Monitor or external non-invasive LT-ECG patch", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Rochester", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2022-02-28", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2025-10-14", "last_synced_at": "2026-11-15T08:00:19.779Z", "location_count": 1, "location_summary": "Rochester, New York", "locations": [ { "city": "Rochester", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04922281" }, { "nct_id": "NCT03183245", "title": "Comparison of the Human Acellular Vessel (HAV) With Fistulas as Conduits for Hemodialysis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Renal Failure", "End Stage Renal Disease", "Hemodialysis", "Vascular Access" ], "interventions": [ { "name": "Human Acellular Vessel (HAV)", "type": "BIOLOGICAL" }, { "name": "Arteriovenous fistula (AVF)", "type": "PROCEDURE" }, { "name": "Hemodialysis", "type": "OTHER" } ], "intervention_types": [ "BIOLOGICAL", "PROCEDURE", "OTHER" ], "sponsor": "Humacyte, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 242, "start_date": "2017-09-29", "completion_date": "2025-06-19", "has_results": false, "last_update_posted_date": "2025-11-20", "last_synced_at": "2026-11-15T08:00:19.779Z", "location_count": 31, "location_summary": "Phoenix, Arizona • Tucson, Arizona • Irvine, California + 27 more", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Tucson", "state": "Arizona" }, { "city": "Irvine", "state": "California" }, { "city": "La Jolla", "state": "California" }, { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03183245" }, { "nct_id": "NCT01202981", "title": "Impact of Glistenings in AcrySof Intraocular Lenses on Visual Quality", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Lenses, Intraocular", "Glistenings", "Visual Quality" ], "interventions": [], "intervention_types": [], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 200, "start_date": "2010-07", "completion_date": "2013-06", "has_results": false, "last_update_posted_date": "2014-12-11", "last_synced_at": "2026-11-15T08:00:19.779Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT01202981" }, { "nct_id": "NCT04678817", "title": "Same Day Oral EC and Implant Initiation", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Contraception" ], "interventions": [ { "name": "Etonogestrel contraceptive implant with oral levonorgestrel", "type": "DEVICE" }, { "name": "Levonorgestrel intrauterine device", "type": "DEVICE" }, { "name": "Copper T380A intrauterine device", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "35 Years", "sex": "FEMALE", "summary": "18 Years to 35 Years · Female only" }, "enrollment_count": 306, "start_date": "2021-02-17", "completion_date": "2024-03-15", "has_results": true, "last_update_posted_date": "2025-04-15", "last_synced_at": "2026-11-15T08:00:19.779Z", "location_count": 2, "location_summary": "Salt Lake City, Utah • West Valley City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" }, { "city": "West Valley City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT04678817" }, { "nct_id": "NCT05128682", "title": "Acute Pudendal Nerve Stimulation On Leak Point Pressure In Women Urodynamic Early Feasibility Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Urinary Incontinence" ], "interventions": [ { "name": "Urodynamic testing with and without pudendal nerve stimulation", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Corewell Health East", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "FEMALE", "summary": "18 Years to 85 Years · Female only" }, "enrollment_count": 4, "start_date": "2022-05-24", "completion_date": "2022-09-07", "has_results": true, "last_update_posted_date": "2023-05-16", "last_synced_at": "2026-11-15T08:00:19.779Z", "location_count": 2, "location_summary": "Royal Oak, Michigan", "locations": [ { "city": "Royal Oak", "state": "Michigan" }, { "city": "Royal Oak", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT05128682" }, { "nct_id": "NCT06823089", "title": "Early Feasibility Study of Cartilage Defect Repair", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Osteoarthritis, Hip", "Femoroacetabular Impingement", "Osteonecrosis", "Legg-Calvé-Perthes Disease", "Osteochondral Lesion", "Hip Dysplasia" ], "interventions": [ { "name": "ReNew Hip Implant", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Cytex Therapeutics, Inc.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "14 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "14 Years to 64 Years" }, "enrollment_count": 15, "start_date": "2025-11-06", "completion_date": "2031-10", "has_results": false, "last_update_posted_date": "2026-09-16", "last_synced_at": "2026-11-15T08:00:19.779Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT06823089" }, { "nct_id": "NCT01129635", "title": "Optimal Coronary Sinus Lead Implantation Using Intracardiac Impedography and Magnetic Resonance Imaging", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Heart Failure, Systolic", "Left Bundle Branch Block" ], "interventions": [ { "name": "Cardiac Resynchronization Therapy (CRT) implantation", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 38, "start_date": "2010-06", "completion_date": "2014-12", "has_results": false, "last_update_posted_date": "2015-01-21", "last_synced_at": "2026-11-15T08:00:19.779Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01129635" }, { "nct_id": "NCT03364660", "title": "Task-specific Epidural Stimulation Study", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injuries" ], "interventions": [ { "name": "Acute epidural stimulation for cardiovascular stability", "type": "DEVICE" }, { "name": "Long Term Epidural Stimulation for Cardiovascular Stability", "type": "DEVICE" }, { "name": "Participants undergo approximately 4 months of epidural stimulation for voluntary movement.", "type": "DEVICE" }, { "name": "Long Term Epidural Stimulation for Cardiovascular Stability plus Stand Training", "type": "DEVICE" }, { "name": "Participants undergo approximately 4 months of epidural stimulation for voluntary movement plus stand training.", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Louisville", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 36, "start_date": "2017-11-08", "completion_date": "2024-12-30", "has_results": false, "last_update_posted_date": "2024-08-28", "last_synced_at": "2026-11-15T08:00:19.779Z", "location_count": 1, "location_summary": "Louisville, Kentucky", "locations": [ { "city": "Louisville", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT03364660" }, { "nct_id": "NCT01940185", "title": "A Post-Approval Study of the LINX® Reflux Management System", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Gastroesophageal Reflux Disease (GERD)" ], "interventions": [ { "name": "LINX device", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Torax Medical Incorporated", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 200, "start_date": "2012-06-30", "completion_date": "2023-06-30", "has_results": false, "last_update_posted_date": "2024-01-05", "last_synced_at": "2026-11-15T08:00:19.779Z", "location_count": 19, "location_summary": "Los Angeles, California • San Diego, California • Englewood, Colorado + 16 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "San Diego", "state": "California" }, { "city": "Englewood", "state": "Colorado" }, { "city": "Albany", "state": "Georgia" }, { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01940185" }, { "nct_id": "NCT01016314", "title": "Efficacy of the Aspen Spinous Process System in Anterior Lumbar Interbody Fusion (ALIF)", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Degenerative Disc Disease" ], "interventions": [ { "name": "Aspen Spinous Process System", "type": "DEVICE" }, { "name": "Pedicle Screw Fixation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Zimmer Biomet", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 0, "start_date": "2009-11", "completion_date": "2016-01", "has_results": false, "last_update_posted_date": "2019-01-23", "last_synced_at": "2026-11-15T08:00:19.779Z", "location_count": 5, "location_summary": "Pomona, California • Sacramento, California • Kansas City, Kansas + 2 more", "locations": [ { "city": "Pomona", "state": "California" }, { "city": "Sacramento", "state": "California" }, { "city": "Kansas City", "state": "Kansas" }, { "city": "New York", "state": "New York" }, { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01016314" } ] }