{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=standard+of+care+treatment&page=13", "query": { "intervention": "standard of care treatment", "page": 13 }, "page_size": 10 }, "pagination": { "page": 13, "page_size": 10, "total_count": 9581, "total_pages": 959, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=standard+of+care+treatment&page=14&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=standard+of+care+treatment&page=12&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-14T02:18:47.571Z", "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{ "nct_id": "NCT03592082", "title": "Use of Bismuth Subsalicylate in Clostridium Difficile Colitis", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Clostridium Difficile Infection" ], "interventions": [ { "name": "Bismuth Subsalicylate", "type": "DRUG" }, { "name": "standard antibiotic therapy", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Bassett Healthcare", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2018-03-01", "completion_date": "2018-07-01", "has_results": false, "last_update_posted_date": "2018-07-19", "last_synced_at": "2026-10-14T02:18:47.571Z", "location_count": 1, "location_summary": "Cooperstown, New York", "locations": [ { "city": "Cooperstown", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03592082" }, { "nct_id": "NCT06534359", "title": "Transpyloric Versus Gastric Feeding in Bronchopulmonary Dysplasia", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Bronchopulmonary Dysplasia", "Gastroesophageal Reflux" ], "interventions": [ { "name": "Transpyloric tube feeding", "type": "OTHER" }, { "name": "Gastric tube feeding", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Children's Hospital of Philadelphia", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "1 Month", "maximum_age": "12 Months", "sex": "ALL", "summary": "1 Month to 12 Months" }, "enrollment_count": 60, "start_date": "2025-07-15", "completion_date": "2027-06-30", "has_results": false, "last_update_posted_date": "2026-07-17", "last_synced_at": "2026-10-14T02:18:47.571Z", "location_count": 4, "location_summary": "Palo Alto, California • Denver, Colorado • Kansas City, Missouri + 1 more", "locations": [ { "city": "Palo Alto", "state": "California" }, { "city": "Denver", "state": "Colorado" }, { "city": "Kansas City", "state": "Missouri" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06534359" }, { "nct_id": "NCT03860259", "title": "Auriculotherapy for Surgical Pain", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Pain", "Surgery", "Shoulder Pain" ], "interventions": [ { "name": "Auriculotherapy cryopuncture device without nitrogen gas", "type": "DEVICE" }, { "name": "Auriculotherapy cryopuncture device with nitrogen gas", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Jacques E. Chelly", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 50, "start_date": "2020-01-24", "completion_date": "2021-09-29", "has_results": true, "last_update_posted_date": "2022-03-17", "last_synced_at": "2026-10-14T02:18:47.571Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03860259" }, { "nct_id": "NCT06992427", "title": "High-dose Prophylactic Gabapentin (HOPE) vs. Placebo to Prevent Opioid Use for Oral Mucositis Pain During Concurrent Chemoradiation for Head and Neck Cancer", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Head and Neck Squamous Cell Carcinoma", "Stage I Head and Neck Cutaneous Squamous Cell Carcinoma AJCC v8", "Stage II Head and Neck Cutaneous Squamous Cell Carcinoma AJCC v8", "Stage III Head and Neck Cutaneous Squamous Cell Carcinoma AJCC v8", "Stage IV Head and Neck Cutaneous Squamous Cell Carcinoma AJCC v8" ], "interventions": [ { "name": "Gabapentin", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Chemotheraphy", "type": "DRUG" }, { "name": "Radiation Therapy", "type": "RADIATION" }, { "name": "Analgesic Agent", "type": "DRUG" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Survey Administration", "type": "OTHER" } ], "intervention_types": [ "DRUG", "RADIATION", "PROCEDURE", "OTHER" ], "sponsor": "Alliance for Clinical Trials in Oncology", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 228, "start_date": "2025-06-05", "completion_date": "2031-04-15", "has_results": false, "last_update_posted_date": "2026-10-02", "last_synced_at": "2026-10-14T02:18:47.571Z", "location_count": 212, "location_summary": "Gilbert, Arizona • Peoria, Arizona • Phoenix, Arizona + 171 more", "locations": [ { "city": "Gilbert", "state": "Arizona" }, { "city": "Peoria", "state": "Arizona" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Phoenix", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT06992427" }, { "nct_id": "NCT07098286", "title": "Enhancing Resilience Among Patients With Stroke: Implementation of High Intensity Home-based Rehabilitation", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Stroke", "Stroke Rehabilitation" ], "interventions": [ { "name": "high intensity home-based rehabilitation", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "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": 500, "start_date": "2025-08-25", "completion_date": "2028-07-31", "has_results": false, "last_update_posted_date": "2026-08-05", "last_synced_at": "2026-10-14T02:18:47.571Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT07098286" }, { "nct_id": "NCT07139990", "title": "Personalized Radiotherapy for Individualized Treatment Strategies and Monitoring (PRISM)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Small Cell Lung Cancer Extensive Stage", "Brain Metastases", "Solid Tumor, Adult", "Thoracic Cancer", "Sarcoma,Soft Tissue", "HNPCC" ], "interventions": [ { "name": "Cohort A: Extensive Stage Small Cell Lung Cancer (ES-SCLC) Thoracic Tumor PULSAR (Personalized ultrahypofractionated stereotactic ablative radiotherapy)", "type": "RADIATION" }, { "name": "Cohort B: Brain metastasis PULSAR (Personalized ultrahypofractionated stereotactic ablative radiotherapy)", "type": "RADIATION" }, { "name": "Cohort C: Sarcoma Pre-Operative PULSAR", "type": "RADIATION" }, { "name": "Cohort D: Resectable Head & Neck Squamous Cell Carcinoma (HNSCC) PULSAR/SAbR", "type": "RADIATION" } ], "intervention_types": [ "RADIATION" ], "sponsor": "University of Texas Southwestern 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": 105, "start_date": "2025-10-28", "completion_date": "2032-09-01", "has_results": false, "last_update_posted_date": "2026-08-17", "last_synced_at": "2026-10-14T02:18:47.571Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07139990" }, { "nct_id": "NCT05139797", "title": "Artificial Intelligence Guided Echocardiographic Screening of Rare Diseases (EchoNet-Screening)", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cardiac Amyloidosis" ], "interventions": [ { "name": "EchoNet-LVH screening for cardiac amyloidosis", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Cedars-Sinai 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": 300, "start_date": "2021-11-18", "completion_date": "2027-06-01", "has_results": false, "last_update_posted_date": "2026-07-22", "last_synced_at": "2026-10-14T02:18:47.571Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05139797" }, { "nct_id": "NCT01066624", "title": "Comparative Trial of Cryotherapy Versus Caphosol Versus Saline Solution Mouth Washes for the Prevention of Oral Mucositis in Patients With Multiple Myeloma Undergoing Hematopoietic Stem Cell Transplantation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mucositis", "Multiple Myeloma" ], "interventions": [ { "name": "0.9% Sodium Chloride irrigation solution", "type": "DRUG" }, { "name": "Cryotherapy (ice chips)", "type": "OTHER" }, { "name": "Calcium phosphate (Caphosol) Ca2+/PO43- mouth rinse", "type": "DEVICE" } ], "intervention_types": [ "DRUG", "OTHER", "DEVICE" ], "sponsor": "The University of Texas Health Science Center at San Antonio", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 117, "start_date": "2009-08", "completion_date": "2014-01", "has_results": true, "last_update_posted_date": "2015-07-23", "last_synced_at": "2026-10-14T02:18:47.571Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01066624" }, { "nct_id": "NCT01524146", "title": "Photodynamic Therapy (PDT) Cholangiocarcinoma Registry", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Unresectable Cholangiocarcinoma", "Biliary Obstruction", "Stent Obstruction", "Biliary Stricture" ], "interventions": [ { "name": "Photodynamic Therapy", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Weill Medical College of Cornell University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 200, "start_date": "2011-11", "completion_date": "2018-12-30", "has_results": false, "last_update_posted_date": "2017-02-20", "last_synced_at": "2026-10-14T02:18:47.571Z", "location_count": 2, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01524146" }, { "nct_id": "NCT07868588", "title": "Leveraging Interventions for Caregiver Growth, Health, Training, Empowerment and Navigation: Comparing Group Behavioral Interventions to Improve Dementia Caregiver Strain", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Elevated Caregiver Strain", "Dementia Caregiver", "Caregiver Stress" ], "interventions": [ { "name": "Caring Together", "type": "BEHAVIORAL" }, { "name": "Savvy Caregiver", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 450, "start_date": "2026-10-05", "completion_date": "2031-07-01", "has_results": false, "last_update_posted_date": "2026-10-09", "last_synced_at": "2026-10-14T02:18:47.571Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07868588" } ] }