{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Quick+Test&page=19", "query": { "intervention": "Quick Test", "page": 19 }, "page_size": 10 }, "pagination": { "page": 19, "page_size": 10, "total_count": 614, "total_pages": 62, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Quick+Test&page=20&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Quick+Test&page=18&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-22T03:10:28.036Z", "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": "NCT04134754", "title": "Carbon Dioxide (CO2) Chemosensitivity and SUDEP", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Epilepsy", "SUDEP" ], "interventions": [ { "name": "6% Carbon dioxide/50% oxygen/balance nitrogen mixture", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Iowa", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 335, "start_date": "2019-12-12", "completion_date": "2029-10-01", "has_results": false, "last_update_posted_date": "2026-06-23", "last_synced_at": "2026-10-22T03:10:28.036Z", "location_count": 1, "location_summary": "Iowa City, Iowa", "locations": [ { "city": "Iowa City", "state": "Iowa" } ], "official_url": "https://clinicaltrials.gov/study/NCT04134754" }, { "nct_id": "NCT00938002", "title": "Study to Determine Quicker Methods of Diagnosing Pneumonia Caused by a Breathing Machine in Critically Ill Patients", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Ventilator Acquired Pneumonia" ], "interventions": [ { "name": "Acceler8 Pheno", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Denver Health and Hospital Authority", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 37, "start_date": "2009-07", "completion_date": "2019-09-19", "has_results": false, "last_update_posted_date": "2019-12-24", "last_synced_at": "2026-10-22T03:10:28.036Z", "location_count": 1, "location_summary": "Denver, Colorado", "locations": [ { "city": "Denver", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT00938002" }, { "nct_id": "NCT05142241", "title": "Testing the Combination of Anti-Cancer Drugs Talazoparib and Temozolomide in Patients With Advanced Stage Rare Cancers, RARE 2 Trial", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Malignant Solid Neoplasm" ], "interventions": [ { "name": "Biopsy Procedure", "type": "PROCEDURE" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Talazoparib", "type": "DRUG" }, { "name": "Temozolomide", "type": "DRUG" } ], "intervention_types": [ "PROCEDURE", "DRUG" ], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "12 Years", "maximum_age": null, "sex": "ALL", "summary": "12 Years and older" }, "enrollment_count": 14, "start_date": "2022-07-11", "completion_date": "2027-09-23", "has_results": true, "last_update_posted_date": "2026-10-14", "last_synced_at": "2026-10-22T03:10:28.036Z", "location_count": 2, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" }, { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT05142241" }, { "nct_id": "NCT00534482", "title": "Evaluation of the \"Americans in Motion - Healthy Interventions\" Project", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Physical Activity", "Diet", "Mental Health" ], "interventions": [ { "name": "Enhanced Office", "type": "BEHAVIORAL" }, { "name": "Conventional Office", "type": "BEHAVIORAL" }, { "name": "AIM-HI program with enhanced feedback", "type": "BEHAVIORAL" }, { "name": "AIM-HI program and regular feedback", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "American Academy of Family Physicians", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 950, "start_date": "2007-07", "completion_date": "2009-10", "has_results": false, "last_update_posted_date": "2011-05-10", "last_synced_at": "2026-10-22T03:10:28.036Z", "location_count": 1, "location_summary": "Leawood, Kansas", "locations": [ { "city": "Leawood", "state": "Kansas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00534482" }, { "nct_id": "NCT05021341", "title": "Bioavailability of Berberine and Dihydroberberine and Their Impact on Glycemia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Glycemia" ], "interventions": [ { "name": "Berberine", "type": "DIETARY_SUPPLEMENT" }, { "name": "Dihydroberberine 200", "type": "DIETARY_SUPPLEMENT" }, { "name": "Dihydroberberine 100", "type": "DIETARY_SUPPLEMENT" }, { "name": "Placebo", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "Lindenwood University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "MALE", "summary": "18 Years to 45 Years · Male only" }, "enrollment_count": 5, "start_date": "2020-06-22", "completion_date": "2020-11-04", "has_results": false, "last_update_posted_date": "2021-08-25", "last_synced_at": "2026-10-22T03:10:28.036Z", "location_count": 1, "location_summary": "Saint Charles, Missouri", "locations": [ { "city": "Saint Charles", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT05021341" }, { "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": "2026-10-22T03:10:28.036Z", "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": "NCT07781423", "title": "Nurse-Led PrEP Initiation Among Incarcerated Individuals", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Prevention Program", "Pre-Exposure Prophylaxis (PrEP)" ], "interventions": [ { "name": "Nurse-Led Intervention", "type": "BEHAVIORAL" }, { "name": "Patient Navigation Intervention", "type": "BEHAVIORAL" }, { "name": "Standard-of-care (SoC)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Rhode Island Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 90, "start_date": "2026-09-01", "completion_date": "2028-04-30", "has_results": false, "last_update_posted_date": "2026-08-24", "last_synced_at": "2026-10-22T03:10:28.036Z", "location_count": 1, "location_summary": "Providence, Rhode Island", "locations": [ { "city": "Providence", "state": "Rhode Island" } ], "official_url": "https://clinicaltrials.gov/study/NCT07781423" }, { "nct_id": "NCT03423862", "title": "Development of Predictive Biomarkers", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Type1diabetes" ], "interventions": [ { "name": "Mixed Meal Tolerance Test", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Medical College of Wisconsin", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "5 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "5 Years to 17 Years" }, "enrollment_count": 50, "start_date": "2017-10-01", "completion_date": "2021-09-30", "has_results": false, "last_update_posted_date": "2024-04-19", "last_synced_at": "2026-10-22T03:10:28.036Z", "location_count": 1, "location_summary": "Milwaukee, Wisconsin", "locations": [ { "city": "Milwaukee", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT03423862" }, { "nct_id": "NCT05655546", "title": "ImmunoCARE: Rapid, Accurate COVID Testing to Reduce Hospitalization of Immunocompromised Individuals", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Immunodeficiency", "Immunosuppression", "HIV Infections", "Graft Versus Host Disease", "Leukemia", "Lymphoma", "Cancer", "Multiple Myeloma", "Transplant", "Age-Related Immunodeficiency" ], "interventions": [ { "name": "Access to Cue Health COVID-19 Remote testing and treatment for COVID-19", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Scripps Translational Science Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "18 Years to 120 Years" }, "enrollment_count": 2117, "start_date": "2022-12-22", "completion_date": "2024-06-20", "has_results": true, "last_update_posted_date": "2025-08-08", "last_synced_at": "2026-10-22T03:10:28.036Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05655546" }, { "nct_id": "NCT02561312", "title": "Comparison of Two Methods of Transfusion for Stroke Prevention in Sickle Cell", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Anemia, Sickle Cell", "Sickling Disorder Due to Hemoglobin S" ], "interventions": [ { "name": "Rapid manual partial exchange transfusion", "type": "OTHER" }, { "name": "Simple Transfusion", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Chattanooga-Hamilton County Hospital Authority", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "3 Years", "maximum_age": "25 Years", "sex": "ALL", "summary": "3 Years to 25 Years" }, "enrollment_count": 9, "start_date": "2015-09", "completion_date": "2017-09-30", "has_results": false, "last_update_posted_date": "2018-07-27", "last_synced_at": "2026-10-22T03:10:28.036Z", "location_count": 1, "location_summary": "Chattanooga, Tennessee", "locations": [ { "city": "Chattanooga", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02561312" } ] }