{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Platform&page=17", "query": { "intervention": "Platform", "page": 17 }, "page_size": 10 }, "pagination": { "page": 17, "page_size": 10, "total_count": 2074, "total_pages": 208, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Platform&page=18&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Platform&page=16&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-23T09:52:27.348Z", "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": "NCT00751998", "title": "Spy II Clinical Registry", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Biliary Tract Diseases" ], "interventions": [ { "name": "SpyGlass", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Boston Scientific Corporation", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 297, "start_date": "2006-11", "completion_date": "2009-10", "has_results": true, "last_update_posted_date": "2021-08-19", "last_synced_at": "2026-10-23T09:52:27.348Z", "location_count": 10, "location_summary": "San Francisco, California • Aurora, Colorado • Indianapolis, Indiana + 7 more", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "Aurora", "state": "Colorado" }, { "city": "Indianapolis", "state": "Indiana" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT00751998" }, { "nct_id": "NCT04591249", "title": "Physical Activity Intervention for Patients Following Lumbar Spine Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Degenerative Disorder", "Spinal Stenosis", "Spondylosis" ], "interventions": [ { "name": "Physical activity intervention", "type": "BEHAVIORAL" }, { "name": "Usual care", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Vanderbilt University 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": 16, "start_date": "2020-10-07", "completion_date": "2021-12-01", "has_results": false, "last_update_posted_date": "2022-03-31", "last_synced_at": "2026-10-23T09:52:27.348Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT04591249" }, { "nct_id": "NCT02614443", "title": "Effectiveness and Acceptability of Internet-delivered Treatment for Depression, Anxiety and Stress", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depression", "Anxiety", "Stress" ], "interventions": [ { "name": "Space from Depression", "type": "OTHER" }, { "name": "Space from Anxiety", "type": "OTHER" }, { "name": "Space from Stress", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Silver Cloud Health", "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": "2015-10", "completion_date": "2017-09", "has_results": false, "last_update_posted_date": "2018-09-11", "last_synced_at": "2026-10-23T09:52:27.348Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT02614443" }, { "nct_id": "NCT02646748", "title": "Pembrolizumab Combined With Itacitinib (INCB039110) and/or Pembrolizumab Combined With INCB050465 in Advanced Solid Tumors", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Colorectal Cancer (CRC)", "Endometrial Cancer", "Melanoma", "Head and Neck Cancer", "Lung Cancer", "MMR-deficient Tumors", "Breast Cancer", "Pancreatic Cancer", "Renal Cell Carcinoma (RCC)", "Solid Tumors", "UC (Urothelial Cancer)" ], "interventions": [ { "name": "Pembrolizumab", "type": "DRUG" }, { "name": "itacitinib", "type": "DRUG" }, { "name": "INCB050465", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Incyte Corporation", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 159, "start_date": "2016-01-25", "completion_date": "2020-11-20", "has_results": false, "last_update_posted_date": "2022-03-31", "last_synced_at": "2026-10-23T09:52:27.348Z", "location_count": 17, "location_summary": "San Francisco, California • Santa Monica, California • Washington D.C., District of Columbia + 12 more", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "Santa Monica", "state": "California" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Port Saint Lucie", "state": "Florida" }, { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT02646748" }, { "nct_id": "NCT05923684", "title": "NLP-Based Feedback to Improve Risk Comms and Informed Shared Decision Making", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Prostate Cancer" ], "interventions": [ { "name": "NLP-based Feedback", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Cedars-Sinai Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 30, "start_date": "2023-11-15", "completion_date": "2027-07-15", "has_results": false, "last_update_posted_date": "2026-08-12", "last_synced_at": "2026-10-23T09:52:27.348Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05923684" }, { "nct_id": "NCT04600011", "title": "Telerehabilitation for Parkinson's Disease", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Parkinson Disease", "Telemedicine" ], "interventions": [ { "name": "Physical and occupational therapy (PT/OT)", "type": "OTHER" }, { "name": "Home Safety Evaluation (HSE)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Rush University 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": 15, "start_date": "2020-01-21", "completion_date": "2021-06-15", "has_results": false, "last_update_posted_date": "2021-09-16", "last_synced_at": "2026-10-23T09:52:27.348Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT04600011" }, { "nct_id": "NCT06380075", "title": "COmparison of Clarus and Optos Ultrawide Field Imaging Systems for Inherited Retinal Disease", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Retinal Disease" ], "interventions": [ { "name": "Spectralis FAF imaging", "type": "DEVICE" }, { "name": "Optos imaging", "type": "DEVICE" }, { "name": "Clarus imaging", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Wisconsin, Madison", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 50, "start_date": "2024-08-29", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2026-04-24", "last_synced_at": "2026-10-23T09:52:27.348Z", "location_count": 1, "location_summary": "Madison, Wisconsin", "locations": [ { "city": "Madison", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT06380075" }, { "nct_id": "NCT07124728", "title": "Syntrillo Telehealth Stroke Risk Reduction Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypertension", "Hypertension (HTN)", "Stroke Prevention", "Cardiovascular Risk Factor" ], "interventions": [ { "name": "Technology-enabled Telehealth Care Plan", "type": "BEHAVIORAL" }, { "name": "Blood Pressure Monitoring Device", "type": "DEVICE" }, { "name": "Tenovi Smart Pillbox", "type": "DEVICE" }, { "name": "Wearable Activity Trackers (Fitbit or Apple Watch)", "type": "DEVICE" }, { "name": "Healthie EHR", "type": "OTHER" }, { "name": "Secure Messaging Platforms (TigerConnect, Weave, AirCall)", "type": "OTHER" }, { "name": "Antihypertensive Medication Management", "type": "DRUG" }, { "name": "Statin Medication Management", "type": "DRUG" }, { "name": "Antiplatelet or Anticoagulant Therapy", "type": "DRUG" }, { "name": "Laboratory Blood Test Collection", "type": "PROCEDURE" } ], "intervention_types": [ "BEHAVIORAL", "DEVICE", "OTHER", "DRUG", "PROCEDURE" ], "sponsor": "Syntrillo, Inc", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": null, "sex": "ALL", "summary": "30 Years and older" }, "enrollment_count": 11, "start_date": "2025-07-30", "completion_date": "2026-07-22", "has_results": false, "last_update_posted_date": "2026-07-30", "last_synced_at": "2026-10-23T09:52:27.348Z", "location_count": 1, "location_summary": "Charlottesville, Virginia", "locations": [ { "city": "Charlottesville", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07124728" }, { "nct_id": "NCT04630431", "title": "Understanding Challenges, Behavioral Patterns, and Preferences Toward Participation in Clinical Trials in Minority Patient Populations: Development of a Personalized Clinical Trial Educational Platform to Increase Participation in Clinical Trials Among Underserved Cancer Patients", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hematopoietic and Lymphoid Cell Neoplasm", "Malignant Solid Neoplasm" ], "interventions": [ { "name": "Best Practice", "type": "OTHER" }, { "name": "Educational Intervention", "type": "OTHER" }, { "name": "Electronic Health Record Review", "type": "OTHER" }, { "name": "Patient Navigation", "type": "BEHAVIORAL" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 590, "start_date": "2019-10-15", "completion_date": "2022-04-12", "has_results": false, "last_update_posted_date": "2026-06-04", "last_synced_at": "2026-10-23T09:52:27.348Z", "location_count": 3, "location_summary": "Scottsdale, Arizona • Jacksonville, Florida • Rochester, Minnesota", "locations": [ { "city": "Scottsdale", "state": "Arizona" }, { "city": "Jacksonville", "state": "Florida" }, { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT04630431" }, { "nct_id": "NCT03442192", "title": "A Comparative Effectiveness Demonstration Project for Linkage and Retention in PrEP Care for Men Who Have Sex With Men", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Adherence, Patient" ], "interventions": [ { "name": "PrEP Care Anywhere Services", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "MALE", "summary": "18 Years to 99 Years · Male only" }, "enrollment_count": 20, "start_date": "2018-07-30", "completion_date": "2021-12-31", "has_results": false, "last_update_posted_date": "2022-12-09", "last_synced_at": "2026-10-23T09:52:27.348Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT03442192" } ] }