{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Test%2FControl&page=54", "query": { "intervention": "Test/Control", "page": 54 }, "page_size": 10 }, "pagination": { "page": 54, "page_size": 10, "total_count": 4498, "total_pages": 450, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Test%2FControl&page=55&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Test%2FControl&page=53&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-27T20:02:22.203Z", "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": "NCT02725060", "title": "Autoimmune Basis for Postural Tachycardia Syndrome", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postural Orthostatic Tachycardia Syndrome", "Postural Tachycardia Syndrome", "Tachycardia", "Arrhythmias, Cardiac", "Autonomic Nervous System Diseases", "Orthostatic Intolerance", "Cardiovascular Diseases", "Primary Dysautonomias" ], "interventions": [ { "name": "phenylephrine", "type": "DRUG" }, { "name": "isoproterenol", "type": "DRUG" }, { "name": "25 micro-Ci of radiation", "type": "RADIATION" }, { "name": "Posture study with blood samples", "type": "PROCEDURE" }, { "name": "24-hour heart rhythm and blood pressure monitoring", "type": "PROCEDURE" }, { "name": "Quantitative Axonal Sudomotor Reflex Testing", "type": "PROCEDURE" }, { "name": "Autonomic function tests", "type": "PROCEDURE" }, { "name": "Rebreathing test", "type": "OTHER" }, { "name": "Assessment of splanchnic capacitance", "type": "OTHER" }, { "name": "microneurography", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "RADIATION", "PROCEDURE", "OTHER" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "18 Years to 50 Years" }, "enrollment_count": 58, "start_date": "2016-02", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2025-11-12", "last_synced_at": "2026-10-27T20:02:22.203Z", "location_count": 2, "location_summary": "Oklahoma City, Oklahoma • Nashville, Tennessee", "locations": [ { "city": "Oklahoma City", "state": "Oklahoma" }, { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02725060" }, { "nct_id": "NCT01573546", "title": "ENLIGHTEN: Exercise and NutritionaL Interventions for coGnitive and Cardiovascular HealTh ENhancement", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cognitive Impairment, no Dementia (CIND)" ], "interventions": [ { "name": "Aerobic Exercise", "type": "BEHAVIORAL" }, { "name": "DASH diet", "type": "BEHAVIORAL" }, { "name": "Health education control", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "55 Years", "maximum_age": null, "sex": "ALL", "summary": "55 Years and older" }, "enrollment_count": 160, "start_date": "2011-12", "completion_date": "2018-03", "has_results": false, "last_update_posted_date": "2018-04-18", "last_synced_at": "2026-10-27T20:02:22.203Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT01573546" }, { "nct_id": "NCT03681808", "title": "Evaluate the Safety and Effectiveness of the Biotrue ONEday for Astigmatism", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Astigmatism" ], "interventions": [ { "name": "Control", "type": "DEVICE" }, { "name": "Test", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Bausch & Lomb Incorporated", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 242, "start_date": "2018-10-10", "completion_date": "2019-12-16", "has_results": true, "last_update_posted_date": "2021-01-08", "last_synced_at": "2026-10-27T20:02:22.203Z", "location_count": 13, "location_summary": "Irvine, California • San Diego, California • San Francisco, California + 9 more", "locations": [ { "city": "Irvine", "state": "California" }, { "city": "San Diego", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "San Jose", "state": "California" }, { "city": "Sunnyvale", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03681808" }, { "nct_id": "NCT03222908", "title": "Perioperative Smoking Cessation Interventions", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Smoking Cessation", "Perioperative/Postoperative Complications" ], "interventions": [ { "name": "Intervention1: Contract Agreement", "type": "BEHAVIORAL" }, { "name": "Intervention2: Implementation Intentions", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 19, "start_date": "2017-08-15", "completion_date": "2018-07-30", "has_results": false, "last_update_posted_date": "2018-12-26", "last_synced_at": "2026-10-27T20:02:22.203Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03222908" }, { "nct_id": "NCT01923350", "title": "Avoiding Diabetes After Pregnancy Trial", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Weight Reduction" ], "interventions": [ { "name": "Weight Reduction Intervention", "type": "BEHAVIORAL" }, { "name": "Weight Reduction Control Arm", "type": "BEHAVIORAL" }, { "name": "Tested for diabetes", "type": "BEHAVIORAL" }, { "name": "Not tested for diabetes", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Social & Scientific Systems Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 140, "start_date": "2011-12", "completion_date": "2013-03", "has_results": false, "last_update_posted_date": "2013-08-15", "last_synced_at": "2026-10-27T20:02:22.203Z", "location_count": 1, "location_summary": "Silver Spring, Maryland", "locations": [ { "city": "Silver Spring", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT01923350" }, { "nct_id": "NCT02598674", "title": "Severe Sepsis in Children - IMPRESS-C", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Acute Kidney Injury", "Chronic Kidney Disease", "Hypertension" ], "interventions": [ { "name": "Iodohippurate", "type": "DRUG" }, { "name": "24 hour ambulatory Blood Pressure", "type": "PROCEDURE" }, { "name": "Peripheral Arterial Tonometry", "type": "PROCEDURE" }, { "name": "Pulse Wave Velocity", "type": "PROCEDURE" }, { "name": "Gadolinium", "type": "DRUG" } ], "intervention_types": [ "DRUG", "PROCEDURE" ], "sponsor": "University of Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "7 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "7 Years to 17 Years" }, "enrollment_count": 0, "start_date": "2019-10", "completion_date": "2021-09", "has_results": false, "last_update_posted_date": "2020-12-09", "last_synced_at": "2026-10-27T20:02:22.203Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02598674" }, { "nct_id": "NCT05846282", "title": "Students Rising Above: Offsetting the Health and Mental Health Costs of Resilience", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Internalizing Mental Health Symptoms", "Allostatic Load", "Health Complaints" ], "interventions": [ { "name": "STRIVE", "type": "BEHAVIORAL" }, { "name": "Study Skills", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "13 Years", "maximum_age": null, "sex": "ALL", "summary": "13 Years and older" }, "enrollment_count": 504, "start_date": "2023-01-09", "completion_date": "2027-06", "has_results": false, "last_update_posted_date": "2026-03-06", "last_synced_at": "2026-10-27T20:02:22.203Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05846282" }, { "nct_id": "NCT04888988", "title": "Testing the Effects of Exercise on Chemotherapy-Induced Peripheral Neuropathy", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chemotherapy-Induced Peripheral Neuropathy", "Hematopoietic and Lymphoid Cell Neoplasm", "Malignant Solid Neoplasm" ], "interventions": [ { "name": "Best Practice", "type": "OTHER" }, { "name": "Exercise Counseling", "type": "OTHER" }, { "name": "Exercise Intervention", "type": "OTHER" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Neuropathy Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER", "PROCEDURE" ], "sponsor": "University of Rochester NCORP Research Base", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 133, "start_date": "2022-02-25", "completion_date": "2027-01-31", "has_results": false, "last_update_posted_date": "2026-09-29", "last_synced_at": "2026-10-27T20:02:22.203Z", "location_count": 93, "location_summary": "Fresno, California • Martinez, California • Roseville, California + 70 more", "locations": [ { "city": "Fresno", "state": "California" }, { "city": "Martinez", "state": "California" }, { "city": "Roseville", "state": "California" }, { "city": "Sacramento", "state": "California" }, { "city": "Sacramento", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04888988" }, { "nct_id": "NCT02363842", "title": "Trial Comparing SOC +Skin IQ MCM vs SOC for Pressure Ulcer (PU)", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pressure Ulcer" ], "interventions": [ { "name": "Skin IQ™ MCM Coverlet", "type": "DEVICE" }, { "name": "Pressure redistribution surface", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Arjohuntleigh", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 160, "start_date": "2015-04", "completion_date": "2016-02", "has_results": false, "last_update_posted_date": "2015-08-14", "last_synced_at": "2026-10-27T20:02:22.203Z", "location_count": 3, "location_summary": "Oklahoma City, Oklahoma • Dallas, Texas • Charlottesville, Virginia", "locations": [ { "city": "Oklahoma City", "state": "Oklahoma" }, { "city": "Dallas", "state": "Texas" }, { "city": "Charlottesville", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT02363842" }, { "nct_id": "NCT03698708", "title": "Cognitive Adaptations to Reduce Emotional Stress Associated With Type 1 Diabetes", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Type 1 Diabetes Mellitus" ], "interventions": [ { "name": "CARES Intervention", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Kansas Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "5 Years", "maximum_age": "12 Years", "sex": "ALL", "summary": "5 Years to 12 Years" }, "enrollment_count": 37, "start_date": "2019-01-20", "completion_date": "2020-07-31", "has_results": true, "last_update_posted_date": "2022-02-11", "last_synced_at": "2026-10-27T20:02:22.203Z", "location_count": 1, "location_summary": "Kansas City, Missouri", "locations": [ { "city": "Kansas City", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT03698708" } ] }