{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Device+B&page=7", "query": { "intervention": "Device B", "page": 7 }, "page_size": 10 }, "pagination": { "page": 7, "page_size": 10, "total_count": 556, "total_pages": 56, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Device+B&page=8&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Device+B&page=6&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-25T11:53:39.377Z", "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": "NCT05539716", "title": "Metabolism and Sleep Apnea Treatment", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obstructive Sleep Apnea", "Fat Disorder" ], "interventions": [ { "name": "PAP Therapy", "type": "DEVICE" }, { "name": "Lifestyle Counseling Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "University of Miami", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 100, "start_date": "2022-05-20", "completion_date": "2027-09-01", "has_results": false, "last_update_posted_date": "2026-03-23", "last_synced_at": "2026-10-25T11:53:39.377Z", "location_count": 1, "location_summary": "Miami, Florida", "locations": [ { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT05539716" }, { "nct_id": "NCT02392806", "title": "Comparative Effectiveness Study of Bubble CPAP Devices in the NICU", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Respiratory Distress Syndrome" ], "interventions": [ { "name": "Bubble CPAP- BabiPlus, Respiralogics", "type": "DEVICE" }, { "name": "Bubble CPAP- B&B Bubbler, B&B Medical devices", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Marya Strand, MD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Day", "maximum_age": "100 Days", "sex": "ALL", "summary": "1 Day to 100 Days" }, "enrollment_count": 43, "start_date": "2015-01", "completion_date": "2016-08", "has_results": true, "last_update_posted_date": "2018-03-09", "last_synced_at": "2026-10-25T11:53:39.377Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT02392806" }, { "nct_id": "NCT00123435", "title": "Veterans Walk for Health Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cardiovascular Diseases", "Diabetes Mellitus", "Hyperlipidemia", "Hypertension", "Obesity" ], "interventions": [ { "name": "Nutritional counseling", "type": "BEHAVIORAL" }, { "name": "Walking program", "type": "BEHAVIORAL" }, { "name": "Simple pedometer", "type": "DEVICE" }, { "name": "Enhanced pedometer", "type": "DEVICE" } ], "intervention_types": [ "BEHAVIORAL", "DEVICE" ], "sponsor": "US Department of Veterans Affairs", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 254, "start_date": "2005-07", "completion_date": "2009-06", "has_results": false, "last_update_posted_date": "2015-08-21", "last_synced_at": "2026-10-25T11:53:39.377Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT00123435" }, { "nct_id": "NCT06541041", "title": "Nerve Transfers Plus Electrical Stimulation to Improve Hand Function in Cervical Spinal Cord Injury", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cervical Spinal Cord Injury", "Cervical Spinal Cord Paralysis", "Tetraplegia", "Tetraplegia/Tetraparesis", "Tetraplegic Spinal Paralysis" ], "interventions": [ { "name": "Brief intraoperative electrical stimulation", "type": "DEVICE" }, { "name": "Temporary Postoperative Peripheral Nerve Stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Stanford University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 10, "start_date": "2025-02-10", "completion_date": "2028-09", "has_results": false, "last_update_posted_date": "2025-02-19", "last_synced_at": "2026-10-25T11:53:39.377Z", "location_count": 1, "location_summary": "Palo Alto, California", "locations": [ { "city": "Palo Alto", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06541041" }, { "nct_id": "NCT01849796", "title": "Transcranial Stimulation (tDCS) For the Treatment of Neuropathic Facial Pain", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Facial Pain" ], "interventions": [ { "name": "tDCS", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Beth Israel Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 21, "start_date": "2010-10", "completion_date": "2013-12", "has_results": false, "last_update_posted_date": "2015-12-10", "last_synced_at": "2026-10-25T11:53:39.377Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01849796" }, { "nct_id": "NCT04949854", "title": "Evaluating the Role of the Guidewire in Peripheral Intravenous Access", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Peripheral Intravenous Vein Catheter Phlebitis", "Intravenous Infection" ], "interventions": [ { "name": "B.Braun 6.35 cm 20 Gauge ultralong intravenous catheter", "type": "DEVICE" }, { "name": "B.D Accucath 5.71 cm 20 Gauge ultralong intravenous catheter", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Corewell Health East", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2023-12", "completion_date": "2023-12", "has_results": false, "last_update_posted_date": "2023-09-18", "last_synced_at": "2026-10-25T11:53:39.377Z", "location_count": 1, "location_summary": "Royal Oak, Michigan", "locations": [ { "city": "Royal Oak", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04949854" }, { "nct_id": "NCT03757091", "title": "Flexible Intubation Scope With or Without Video Laryngoscope in Supporting Endotracheal Tube Placement in Patients With Head and Neck Cancer Before Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Head and Neck Neoplasm" ], "interventions": [ { "name": "Laryngoscopy", "type": "DEVICE" }, { "name": "Tracheal Intubation", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 143, "start_date": "2019-01-15", "completion_date": "2026-02-02", "has_results": true, "last_update_posted_date": "2026-02-18", "last_synced_at": "2026-10-25T11:53:39.377Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03757091" }, { "nct_id": "NCT07679074", "title": "CREST: Samphire Guided Care Program on Wellbeing, Work Productivity, and Quality of Life", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Premenstrual Syndrome", "Premenstrual Dysphoric Disorder", "Dysmenorrhea", "Endometriosis", "Perimenopause", "Menopause", "Pelvic Pain" ], "interventions": [ { "name": "Lutea Transcranial Direct Current Stimulation (tDCS) Device", "type": "DEVICE" }, { "name": "Samphire Guided Care Program", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "Samphire Group, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "FEMALE", "summary": "18 Years to 65 Years · Female only" }, "enrollment_count": 50, "start_date": "2026-06-01", "completion_date": "2027-03-01", "has_results": false, "last_update_posted_date": "2026-07-01", "last_synced_at": "2026-10-25T11:53:39.377Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07679074" }, { "nct_id": "NCT06107361", "title": "Evaluating the Role of the Guidewire in Peripheral Intravenous Access: A Randomized Controlled Trial of Ultrasound-Guided Catheter Survival", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Peripheral Intravenous Vein Catheter Phlebitis", "Intravenous Infection" ], "interventions": [ { "name": "B. Braun 6.35cm 20 gauge ultralong intravenous catheter", "type": "DEVICE" }, { "name": "BD 5.71 cm 20 gauge Accucath", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Corewell Health East", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 360, "start_date": "2023-11-07", "completion_date": "2026-07-31", "has_results": false, "last_update_posted_date": "2026-06-10", "last_synced_at": "2026-10-25T11:53:39.377Z", "location_count": 1, "location_summary": "Royal Oak, Michigan", "locations": [ { "city": "Royal Oak", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT06107361" }, { "nct_id": "NCT03961295", "title": "A Pilot Study to Compare the Pharmacokinetics (PK) of Single Subcutaneous (SC) Injections of Vedolizumab Administered in Prefilled Syringe (PFS) Versus (vs) Prefilled Syringe in Autoinjector (PFS+AI) in Healthy Participants", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Healthy Volunteers" ], "interventions": [ { "name": "Vedolizumab SC", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Takeda", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 24, "start_date": "2018-02-22", "completion_date": "2018-08-28", "has_results": true, "last_update_posted_date": "2019-11-13", "last_synced_at": "2026-10-25T11:53:39.377Z", "location_count": 1, "location_summary": "Lincoln, Nebraska", "locations": [ { "city": "Lincoln", "state": "Nebraska" } ], "official_url": "https://clinicaltrials.gov/study/NCT03961295" } ] }