{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Paired&page=6", "query": { "intervention": "Paired", "page": 6 }, "page_size": 10 }, "pagination": { "page": 6, "page_size": 10, "total_count": 854, "total_pages": 86, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Paired&page=7&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Paired&page=5&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-20T02:26:19.434Z", "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": "NCT02902835", "title": "BUPrenorphine Facilitated Access and Supportive Treatment --AIM 3", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Opioid-related Disorders" ], "interventions": [ { "name": "BUP_FAST", "type": "BEHAVIORAL" }, { "name": "Referral to treatment", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Montefiore Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 13, "start_date": "2016-09-01", "completion_date": "2018-06-30", "has_results": false, "last_update_posted_date": "2018-09-13", "last_synced_at": "2026-10-20T02:26:19.434Z", "location_count": 1, "location_summary": "The Bronx, New York", "locations": [ { "city": "The Bronx", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02902835" }, { "nct_id": "NCT04190901", "title": "Effect of Physician Race and Gender on Simulated Patients' Ratings", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Bias, Racial", "Bias, Sex", "Patient Satisfaction", "Physician-Patient Relations" ], "interventions": [ { "name": "Simulated Black Male Physician", "type": "BEHAVIORAL" }, { "name": "Simulated Black Female Physician", "type": "BEHAVIORAL" }, { "name": "Simulated White Male Physician", "type": "BEHAVIORAL" }, { "name": "Simulated White Female Physician", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 3592, "start_date": "2018-03-09", "completion_date": "2018-07-31", "has_results": false, "last_update_posted_date": "2020-07-21", "last_synced_at": "2026-10-20T02:26:19.434Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT04190901" }, { "nct_id": "NCT00838981", "title": "Pharmacotherapy & CM for Opioid and Cocaine Dependence", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Cocaine Dependence" ], "interventions": [ { "name": "Modafinil", "type": "DRUG" }, { "name": "Sugar Pill", "type": "DRUG" }, { "name": "Contingency Management", "type": "BEHAVIORAL" }, { "name": "Methadone", "type": "DRUG" }, { "name": "cognitive behavioral treatment", "type": "BEHAVIORAL" }, { "name": "Voucher Control", "type": "BEHAVIORAL" } ], "intervention_types": [ "DRUG", "BEHAVIORAL" ], "sponsor": "Yale 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": 91, "start_date": "2008-05", "completion_date": "2014-03", "has_results": true, "last_update_posted_date": "2021-12-03", "last_synced_at": "2026-10-20T02:26:19.434Z", "location_count": 1, "location_summary": "West Haven, Connecticut", "locations": [ { "city": "West Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT00838981" }, { "nct_id": "NCT03095781", "title": "Pembrolizumab and XL888 in Patients With Advanced Gastrointestinal Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Colorectal Adenocarcinoma", "Metastatic Pancreatic Adenocarcinoma", "Recurrent Colorectal Carcinoma", "Recurrent Pancreatic Carcinoma", "Stage III Colorectal Cancer", "Stage III Pancreatic Cancer", "Stage IIIA Colorectal Cancer", "Stage IIIB Colorectal Cancer", "Stage IV Colorectal Cancer", "Stage IV Pancreatic Cancer", "Stage IVA Colorectal Cancer", "Stage IVA Pancreatic Cancer", "Stage IVB Colorectal Cancer", "Stage IVB Pancreatic Cancer", "Unresectable Pancreatic Carcinoma" ], "interventions": [ { "name": "XL888", "type": "DRUG" }, { "name": "Pembrolizumab", "type": "BIOLOGICAL" } ], "intervention_types": [ "DRUG", "BIOLOGICAL" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 47, "start_date": "2017-07-07", "completion_date": "2021-06-10", "has_results": true, "last_update_posted_date": "2026-05-22", "last_synced_at": "2026-10-20T02:26:19.434Z", "location_count": 3, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" }, { "city": "Atlanta", "state": "Georgia" }, { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT03095781" }, { "nct_id": "NCT06361095", "title": "Confirmatory Efficacy Trial of Attention Bias Modification for Depression", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Depression" ], "interventions": [ { "name": "Traditional Attention Bias Modification", "type": "BEHAVIORAL" }, { "name": "Gamified Attention Bias Modification", "type": "BEHAVIORAL" }, { "name": "Sham Attention Bias Modification", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Texas at Austin", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 600, "start_date": "2024-05-01", "completion_date": "2028-05-01", "has_results": false, "last_update_posted_date": "2025-09-15", "last_synced_at": "2026-10-20T02:26:19.434Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06361095" }, { "nct_id": "NCT03543865", "title": "Southwest Hub for American Indian Youth Suicide Prevention Research", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Suicide", "Surveillance", "Mental Health", "Substance Use", "Depressive Symptoms" ], "interventions": [ { "name": "New Hope (NH)", "type": "BEHAVIORAL" }, { "name": "Elders Resilience (ER)", "type": "BEHAVIORAL" }, { "name": "Case Management (CM)", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Johns Hopkins Bloomberg School of Public Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "16 Years", "maximum_age": "29 Years", "sex": "ALL", "summary": "16 Years to 29 Years" }, "enrollment_count": 304, "start_date": "2019-03-25", "completion_date": "2024-11-30", "has_results": true, "last_update_posted_date": "2026-01-23", "last_synced_at": "2026-10-20T02:26:19.434Z", "location_count": 1, "location_summary": "Whiteriver, Arizona", "locations": [ { "city": "Whiteriver", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT03543865" }, { "nct_id": "NCT07769918", "title": "Hypoxia-targeted Radiotherapy Boost for GBM", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Glioblastoma (GBM)" ], "interventions": [ { "name": "Dynamic susceptibility contrast MRI (DSC-MRI)", "type": "DEVICE" }, { "name": "Cercare Medical Neurosuite (CMN) DSC-MRI-derived hypoxia maps", "type": "OTHER" }, { "name": "Varian TrueBeam", "type": "RADIATION" } ], "intervention_types": [ "DEVICE", "OTHER", "RADIATION" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 25, "start_date": "2026-09-01", "completion_date": "2029-06-01", "has_results": false, "last_update_posted_date": "2026-08-18", "last_synced_at": "2026-10-20T02:26:19.434Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07769918" }, { "nct_id": "NCT07225582", "title": "Development of Optimal Sensory Feedback Strategies to Maximize Function After Tetraplegia", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injury Cervical", "Spinal Cord Injuries (Complete and Incomplete)" ], "interventions": [ { "name": "Brain Computer Interface (BCI) - Functional Electrical Stimulation (FES) system", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Case Western Reserve University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "22 Years to 65 Years" }, "enrollment_count": 3, "start_date": "2026-01-13", "completion_date": "2030-09-01", "has_results": false, "last_update_posted_date": "2026-02-19", "last_synced_at": "2026-10-20T02:26:19.434Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT07225582" }, { "nct_id": "NCT05857527", "title": "Extending taVNS Paired With Infant CIMT Into a Home-Based Setting", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Cerebral Palsy" ], "interventions": [ { "name": "Custom EMG triggered Soterix taVNS stimulation with CIMT therapy in lab", "type": "COMBINATION_PRODUCT" }, { "name": "Custom EMG triggered Soterix taVNS stimulation with CIMT therapy in home", "type": "COMBINATION_PRODUCT" } ], "intervention_types": [ "COMBINATION_PRODUCT" ], "sponsor": "Medical University of South Carolina", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "6 Months", "maximum_age": "18 Months", "sex": "ALL", "summary": "6 Months to 18 Months" }, "enrollment_count": 4, "start_date": "2023-04-17", "completion_date": "2024-03-30", "has_results": true, "last_update_posted_date": "2025-07-04", "last_synced_at": "2026-10-20T02:26:19.434Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05857527" }, { "nct_id": "NCT04588714", "title": "Feasibility and Preliminary Effects of the Resilience-based, Energy Management to Enhance Wellbeing in Systemic Sclerosis (RENEW) Intervention", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Scleroderma" ], "interventions": [ { "name": "Resilience-based, Energy Management to Enhance Wellbeing (RENEW)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 21, "start_date": "2020-10-27", "completion_date": "2021-05-31", "has_results": false, "last_update_posted_date": "2022-09-23", "last_synced_at": "2026-10-20T02:26:19.434Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04588714" } ] }