{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Diagnostic+Cardiac+Imaging&page=2", "query": { "intervention": "Diagnostic Cardiac Imaging", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 469, "total_pages": 47, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Diagnostic+Cardiac+Imaging&page=3&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Diagnostic+Cardiac+Imaging&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-30T09:41:26.856Z", "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": "NCT06694181", "title": "Safe and Explainable AI", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Artifical Inteligence", "Cardiology", "Breast Cancer", "Sepsis" ], "interventions": [ { "name": "AI-PERSONALIZED CLINICAL DECISION SUPPORT", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Abramson Cancer Center at Penn Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 300000, "start_date": "2025-11-29", "completion_date": "2028-11", "has_results": false, "last_update_posted_date": "2026-02-25", "last_synced_at": "2026-09-30T09:41:26.856Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06694181" }, { "nct_id": "NCT05312164", "title": "Physio-Anatomy Clinical Data Collection Study", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Coronary Stenosis" ], "interventions": [ { "name": "HF-OCT Imaging", "type": "DEVICE" }, { "name": "FFR Pressure Wire", "type": "DEVICE" }, { "name": "Angiography", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Gentuity, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": null, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 150, "start_date": "2022-03-14", "completion_date": "2025-12-31", "has_results": false, "last_update_posted_date": "2025-03-20", "last_synced_at": "2026-09-30T09:41:26.856Z", "location_count": 6, "location_summary": "Palo Alto, California • Tampa, Florida • Decatur, Georgia + 3 more", "locations": [ { "city": "Palo Alto", "state": "California" }, { "city": "Tampa", "state": "Florida" }, { "city": "Decatur", "state": "Georgia" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT05312164" }, { "nct_id": "NCT04447027", "title": "Romidepsin, CC-486 (5-azacitidine), Dexamethasone, and Lenalidomide (RAdR) for Relapsed/Refractory T-cell Malignancies", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Cutaneous T-Cell Lymphoma", "Mature T-cell Malignancies", "Peripheral T-Cell Lymphoma", "Relapsed/ Refractory T-cell Malignancies" ], "interventions": [ { "name": "Romidepsin", "type": "DRUG" }, { "name": "Lenalidomide", "type": "DRUG" }, { "name": "CC-486 (5-azacitidine)", "type": "DRUG" }, { "name": "Dexamethasone", "type": "DRUG" }, { "name": "EKG", "type": "DIAGNOSTIC_TEST" }, { "name": "Bone Marrow Aspiration/Biopsy", "type": "PROCEDURE" }, { "name": "MRI", "type": "DIAGNOSTIC_TEST" }, { "name": "Lumbar Puncture", "type": "PROCEDURE" }, { "name": "TTE", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DRUG", "DIAGNOSTIC_TEST", "PROCEDURE" ], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 26, "start_date": "2020-12-17", "completion_date": "2025-12-17", "has_results": true, "last_update_posted_date": "2026-08-13", "last_synced_at": "2026-09-30T09:41:26.856Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT04447027" }, { "nct_id": "NCT04814420", "title": "Atrial Fibrosis in Obstructive Sleep Apnea Patients: A Pilot Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Atrial Fibrillation", "Obstructive Sleep Apnea" ], "interventions": [ { "name": "Delayed enhancement magnetic resonance imaging (DE-MRI)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Tulane University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 60, "start_date": "2021-07-12", "completion_date": "2026-11", "has_results": false, "last_update_posted_date": "2026-06-15", "last_synced_at": "2026-09-30T09:41:26.856Z", "location_count": 3, "location_summary": "New Orleans, Louisiana", "locations": [ { "city": "New Orleans", "state": "Louisiana" }, { "city": "New Orleans", "state": "Louisiana" }, { "city": "New Orleans", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT04814420" }, { "nct_id": "NCT06212791", "title": "EXercise Cardiac Magnetic Resonance Assessment of Left Atrial Mechanics Following Ablation", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Paroxysmal Atrial Fibrillation" ], "interventions": [ { "name": "Self- Report Evaluation-Duke Activity Status Index", "type": "BEHAVIORAL" }, { "name": "Self- Report Evaluation Atrial Fibrillation Effect on Quality of Life Questionnaire", "type": "BEHAVIORAL" }, { "name": "Cardiopulmonary exercise test (CPET)", "type": "DIAGNOSTIC_TEST" }, { "name": "Transthoracic echocardiogram", "type": "DIAGNOSTIC_TEST" }, { "name": "Ambulatory cardiac rhythm assessment", "type": "DIAGNOSTIC_TEST" }, { "name": "Cardiovascular magnetic resonance (CMR)", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "BEHAVIORAL", "DIAGNOSTIC_TEST" ], "sponsor": "Virginia Commonwealth University", "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": "2024-12-26", "completion_date": "2028-03", "has_results": false, "last_update_posted_date": "2026-03-12", "last_synced_at": "2026-09-30T09:41:26.856Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT06212791" }, { "nct_id": "NCT06455488", "title": "MANAGE-VT Registry - MANAGEment of Ventricular Tachycardia Outcomes Registry", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Ventricular Tachycardia" ], "interventions": [ { "name": "Ventricular Tachycardia Ablation", "type": "PROCEDURE" }, { "name": "ICD Implant", "type": "DEVICE" }, { "name": "Antiarrhythmic drug", "type": "DRUG" }, { "name": "EKG", "type": "DIAGNOSTIC_TEST" }, { "name": "Cardioversion", "type": "DIAGNOSTIC_TEST" }, { "name": "Echocardiogram", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "PROCEDURE", "DEVICE", "DRUG", "DIAGNOSTIC_TEST" ], "sponsor": "CorVita Science Foundation", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 130, "start_date": "2020-07-20", "completion_date": "2030-07-20", "has_results": false, "last_update_posted_date": "2024-06-12", "last_synced_at": "2026-09-30T09:41:26.856Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06455488" }, { "nct_id": "NCT07769047", "title": "Semaglutide and Structured Lifestyle Support to Improve Heart and Blood Vessel Health in Postmenopausal Obese Breast Cancer Survivors Taking Aromatase Inhibitors", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Anatomic Stage I Breast Cancer AJCC v8", "Anatomic Stage II Breast Cancer AJCC v8", "Anatomic Stage III Breast Cancer AJCC v8" ], "interventions": [ { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Dual X-ray Absorptiometry", "type": "PROCEDURE" }, { "name": "Functional Assessment", "type": "OTHER" }, { "name": "Lifestyle Counseling", "type": "BEHAVIORAL" }, { "name": "Semaglutide", "type": "DRUG" } ], "intervention_types": [ "PROCEDURE", "OTHER", "BEHAVIORAL", "DRUG" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "46 Years", "maximum_age": "55 Years", "sex": "FEMALE", "summary": "46 Years to 55 Years · Female only" }, "enrollment_count": 50, "start_date": "2026-09-01", "completion_date": "2035-07-30", "has_results": false, "last_update_posted_date": "2026-08-17", "last_synced_at": "2026-09-30T09:41:26.856Z", "location_count": 1, "location_summary": "Jacksonville, Florida", "locations": [ { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT07769047" }, { "nct_id": "NCT03954015", "title": "Comparison of Three Methods for Early Detection of Breast Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Proliferative Breast Disease" ], "interventions": [ { "name": "Contrast Enhanced imaging", "type": "DIAGNOSTIC_TEST" }, { "name": "Lumason", "type": "DRUG" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "DRUG" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": null, "sex": "FEMALE", "summary": "30 Years and older · Female only" }, "enrollment_count": 3, "start_date": "2019-10-15", "completion_date": "2021-10-05", "has_results": false, "last_update_posted_date": "2022-01-10", "last_synced_at": "2026-09-30T09:41:26.856Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT03954015" }, { "nct_id": "NCT05996523", "title": "Phase II Trial of Immunotherapeutic HPV Vaccine PRGN-2009 With Pembrolizumab Before Standard Treatment in Subjects With Newly Diagnosed HPV-Associated Oropharyngeal Cancer", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Oropharyngeal Squamous Cell Carcinoma (SCC)" ], "interventions": [ { "name": "PRGN-2009", "type": "BIOLOGICAL" }, { "name": "Pembrolizumab", "type": "DRUG" }, { "name": "EKG", "type": "DIAGNOSTIC_TEST" }, { "name": "CT", "type": "DIAGNOSTIC_TEST" }, { "name": "PET scan", "type": "DIAGNOSTIC_TEST" }, { "name": "MRI", "type": "DIAGNOSTIC_TEST" }, { "name": "Biopsy", "type": "PROCEDURE" } ], "intervention_types": [ "BIOLOGICAL", "DRUG", "DIAGNOSTIC_TEST", "PROCEDURE" ], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "18 Years to 120 Years" }, "enrollment_count": 26, "start_date": "2023-11-07", "completion_date": "2030-07-16", "has_results": true, "last_update_posted_date": "2026-06-23", "last_synced_at": "2026-09-30T09:41:26.856Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT05996523" }, { "nct_id": "NCT00597974", "title": "Neurological Outcome With Carotid Artery Stenting", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Carotid Artery Disease", "Carotid Artery Stenosis", "Stroke", "Transient Ischemic Attack" ], "interventions": [ { "name": "Angioplasty", "type": "PROCEDURE" }, { "name": "Stent", "type": "DEVICE" }, { "name": "Neurological and neuropsychological evaluations", "type": "OTHER" }, { "name": "Angiography", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE", "DEVICE", "OTHER" ], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 108, "start_date": "2003-09", "completion_date": "2014-04", "has_results": false, "last_update_posted_date": "2015-06-04", "last_synced_at": "2026-09-30T09:41:26.856Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00597974" } ] }