{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sample+collection+only&page=2", "query": { "intervention": "Sample collection only", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sample+collection+only&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-12T04:47:53.082Z", "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": "NCT04709081", "title": "A Drug Interaction Study of ACH-0145228", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Healthy" ], "interventions": [ { "name": "ACH-0145228", "type": "DRUG" }, { "name": "Midazolam", "type": "DRUG" }, { "name": "Digoxin", "type": "DRUG" }, { "name": "Itraconazole", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Alexion Pharmaceuticals, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "18 Years to 55 Years" }, "enrollment_count": 38, "start_date": "2019-12-22", "completion_date": "2020-04-16", "has_results": false, "last_update_posted_date": "2021-01-14", "last_synced_at": "2026-09-12T04:47:53.082Z", "location_count": 1, "location_summary": "Tempe, Arizona", "locations": [ { "city": "Tempe", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT04709081" }, { "nct_id": "NCT03895320", "title": "Protecting Our Future Generation: Promotion of Protective Sexual Health Practices Among Native American Youth and Young Adults Through an Assets-based Self-care Intervention", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sexual Behavior", "Unprotected Sex", "Gonorrhea", "Chlamydia", "Trichomonas", "Sexually Transmitted Diseases", "Adolescent Behavior", "Self Evaluation" ], "interventions": [ { "name": "Sexual Health Risk Assessment", "type": "BEHAVIORAL" }, { "name": "Sexual Health Score", "type": "BEHAVIORAL" }, { "name": "Sexual Health Messaging", "type": "BEHAVIORAL" }, { "name": "Water SSB Quiz", "type": "BEHAVIORAL" }, { "name": "Water SSB Score", "type": "BEHAVIORAL" }, { "name": "Water SSB Messaging", "type": "BEHAVIORAL" }, { "name": "STI Screening", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Johns Hopkins Bloomberg School of Public Health", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "14 Years", "maximum_age": "26 Years", "sex": "ALL", "summary": "14 Years to 26 Years" }, "enrollment_count": 219, "start_date": "2019-03-01", "completion_date": "2022-03-31", "has_results": false, "last_update_posted_date": "2024-02-23", "last_synced_at": "2026-09-12T04:47:53.082Z", "location_count": 1, "location_summary": "Whiteriver, Arizona", "locations": [ { "city": "Whiteriver", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT03895320" }, { "nct_id": "NCT06140407", "title": "Pembrolizumab After Radiation Therapy and Chemotherapy in Limited Stage Small Cell Lung Cancer", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Limited Stage Lung Small Cell Carcinoma", "Stage I Lung Cancer", "Stage II Lung Cancer", "Stage III Lung Cancer" ], "interventions": [ { "name": "Cisplatin", "type": "DRUG" }, { "name": "Carboplatin", "type": "DRUG" }, { "name": "Etoposide", "type": "DRUG" }, { "name": "Pembrolizumab", "type": "BIOLOGICAL" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Positron Emission Tomography", "type": "PROCEDURE" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Radiation Therapy", "type": "RADIATION" } ], "intervention_types": [ "DRUG", "BIOLOGICAL", "PROCEDURE", "RADIATION" ], "sponsor": "Vanderbilt-Ingram Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1, "start_date": "2024-02-14", "completion_date": "2025-05-27", "has_results": false, "last_update_posted_date": "2025-06-05", "last_synced_at": "2026-09-12T04:47:53.082Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT06140407" }, { "nct_id": "NCT01137656", "title": "Storage Lesion in Banked Blood Due to Disruption of Nitric Oxide (NO) Homeostasis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Healthy" ], "interventions": [ { "name": "Acetylcholine and Blood", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Mark Gladwin", "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": 53, "start_date": "2010-04", "completion_date": "2013-09", "has_results": false, "last_update_posted_date": "2015-04-14", "last_synced_at": "2026-09-12T04:47:53.082Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT01137656" }, { "nct_id": "NCT05020002", "title": "Extracellular RNA Biomarkers of Myotonic Dystrophy", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Myotonic Dystrophy" ], "interventions": [], "intervention_types": [], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "5 Years", "maximum_age": null, "sex": "ALL", "summary": "5 Years and older" }, "enrollment_count": 215, "start_date": "2020-12-08", "completion_date": "2027-12", "has_results": false, "last_update_posted_date": "2025-11-24", "last_synced_at": "2026-09-12T04:47:53.082Z", "location_count": 3, "location_summary": "Boston, Massachusetts • Dallas, Texas", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05020002" }, { "nct_id": "NCT07662928", "title": "Epcoritamab in Combination With Dose Adjusted EPOCH-R for High-risk Burkitt Lymphoma (BL), The BEDROCK Study", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Adult Burkitt Lymphoma" ], "interventions": [ { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Bone Marrow Aspiration", "type": "PROCEDURE" }, { "name": "Bone Marrow Biopsy", "type": "PROCEDURE" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Cyclophosphamide", "type": "DRUG" }, { "name": "Doxorubicin", "type": "DRUG" }, { "name": "Echocardiography Test", "type": "PROCEDURE" }, { "name": "Epcoritamab", "type": "BIOLOGICAL" }, { "name": "Etoposide", "type": "DRUG" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Multigated Acquisition Scan", "type": "PROCEDURE" }, { "name": "Positron Emission Tomography", "type": "PROCEDURE" }, { "name": "Prednisone", "type": "DRUG" }, { "name": "Rituximab", "type": "BIOLOGICAL" }, { "name": "Vincristine", "type": "DRUG" } ], "intervention_types": [ "PROCEDURE", "DRUG", "BIOLOGICAL" ], "sponsor": "AIDS Malignancy Consortium", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 43, "start_date": "2026-09-17", "completion_date": "2033-04-30", "has_results": false, "last_update_posted_date": "2026-08-14", "last_synced_at": "2026-09-12T04:47:53.082Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07662928" }, { "nct_id": "NCT06500377", "title": "Comparing the Impact of Four Types of Meditation Practices for Relaxation in Cancer Survivors", "overall_status": "SUSPENDED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hematopoietic and Lymphatic System Neoplasm", "Malignant Solid Neoplasm" ], "interventions": [ { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Meditation Therapy", "type": "PROCEDURE" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "City of Hope 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": 44, "start_date": "2024-06-17", "completion_date": "2027-03-12", "has_results": false, "last_update_posted_date": "2026-09-03", "last_synced_at": "2026-09-12T04:47:53.082Z", "location_count": 2, "location_summary": "Duarte, California • Irvine, California", "locations": [ { "city": "Duarte", "state": "California" }, { "city": "Irvine", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06500377" }, { "nct_id": "NCT06830265", "title": "Comparing Standard of Care Biopsy System to a Novel Biopsy Needle System by Computational Pathologic Analysis", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Prostate Cancer Screening" ], "interventions": [ { "name": "Novel needle biopsy catheter (test)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Uro-1 Medical", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 200, "start_date": "2025-07-07", "completion_date": "2026-12-10", "has_results": false, "last_update_posted_date": "2026-09-04", "last_synced_at": "2026-09-12T04:47:53.082Z", "location_count": 3, "location_summary": "New York, New York • Durham, North Carolina • Hardeeville, South Carolina", "locations": [ { "city": "New York", "state": "New York" }, { "city": "Durham", "state": "North Carolina" }, { "city": "Hardeeville", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06830265" }, { "nct_id": "NCT07291180", "title": "A Feasibility Study of Mass-Based Response Drug Screening to Guide Personalized Hyperthermic Intraperitoneal Chemotherapy for High-Grade Appendiceal and Colorectal Adenocarcinoma With Peritoneal Metastasis", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Appendiceal Cancer", "Colorectal Adenocarcinoma", "Peritoneal Metastases" ], "interventions": [ { "name": "Mass-based response testing (MRT)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "81 Years", "sex": "ALL", "summary": "18 Years to 81 Years" }, "enrollment_count": 20, "start_date": "2026-02-17", "completion_date": "2027-12", "has_results": false, "last_update_posted_date": "2026-07-21", "last_synced_at": "2026-09-12T04:47:53.082Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT07291180" }, { "nct_id": "NCT03132168", "title": "Postoperative Delirium in Patients Undergoing Radical Cystectomy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post-operative Delirium" ], "interventions": [ { "name": "Assessments", "type": "BEHAVIORAL" }, { "name": "Blood Draw", "type": "PROCEDURE" }, { "name": "Standardized Anesthetic Care", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "PROCEDURE", "OTHER" ], "sponsor": "Ohio State 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": "2018-01-10", "completion_date": "2021-01-31", "has_results": false, "last_update_posted_date": "2021-08-27", "last_synced_at": "2026-09-12T04:47:53.082Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03132168" } ] }