{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Usual+clinical+care&page=5", "query": { "intervention": "Usual clinical care", "page": 5 }, "page_size": 10 }, "pagination": { "page": 5, "page_size": 10, "total_count": 1466, "total_pages": 147, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Usual+clinical+care&page=6&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Usual+clinical+care&page=4&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-10T02:16:21.540Z", "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": "NCT05745285", "title": "Leukemia and Lymphoma Society (LLS) Services Impact on Outcomes and Care", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Leukemia", "Lymphoma", "Myeloma", "Myelodysplastic Syndromes", "Myeloproliferative Neoplasm" ], "interventions": [ { "name": "LLS Program", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Miami", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 400, "start_date": "2025-02-04", "completion_date": "2026-11-01", "has_results": false, "last_update_posted_date": "2026-02-20", "last_synced_at": "2026-10-10T02:16:21.540Z", "location_count": 3, "location_summary": "Miami, Florida • Chicago, Illinois • San Antonio, Texas", "locations": [ { "city": "Miami", "state": "Florida" }, { "city": "Chicago", "state": "Illinois" }, { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05745285" }, { "nct_id": "NCT01188070", "title": "Caregiver Stress: Interventions to Promote Health and Wellbeing", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Health Promotion" ], "interventions": [ { "name": "Usual Care", "type": "BEHAVIORAL" }, { "name": "Psycho-education", "type": "BEHAVIORAL" }, { "name": "Psycho-education plus physical exercise", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 354, "start_date": "2010-01", "completion_date": "2014-05", "has_results": false, "last_update_posted_date": "2017-02-23", "last_synced_at": "2026-10-10T02:16:21.540Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01188070" }, { "nct_id": "NCT06593327", "title": "NT-ProBNP-based Heart Failure Screening and Prevention Trial in Patients With Type 2 Diabetes: STRONG-DM Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Type 2 Diabetes", "Diabetic Cardiomyopathy", "Heart Failure", "Cardiometabolic Diseases" ], "interventions": [ { "name": "Intensive Prevention Strategy", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Texas Southwestern Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 300, "start_date": "2025-02-10", "completion_date": "2027-12-15", "has_results": false, "last_update_posted_date": "2026-09-29", "last_synced_at": "2026-10-10T02:16:21.540Z", "location_count": 3, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" }, { "city": "Dallas", "state": "Texas" }, { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06593327" }, { "nct_id": "NCT07504588", "title": "Sacituzumab Govitecan With Bevacizumab Compared to Usual Chemotherapy (Carboplatin, Pegylated Liposomal Doxorubicin and Bevacizumab) for Treating Recurrent Platinum-Sensitive Ovarian Cancer After PARP Inhibitor Maintenance Therapy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Recurrent Platinum-Sensitive Fallopian Tube Endometrioid Adenocarcinoma", "Recurrent Platinum-Sensitive Fallopian Tube High Grade Serous Adenocarcinoma", "Recurrent Platinum-Sensitive Ovarian High Grade Endometrioid Adenocarcinoma", "Recurrent Platinum-Sensitive Ovarian High Grade Serous Adenocarcinoma", "Recurrent Platinum-Sensitive Primary Peritoneal Endometrioid Adenocarcinoma", "Recurrent Platinum-Sensitive Primary Peritoneal High Grade Serous Adenocarcinoma" ], "interventions": [ { "name": "Anti-VEGF Monoclonal Antibody", "type": "BIOLOGICAL" }, { "name": "Bevacizumab", "type": "BIOLOGICAL" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Carboplatin", "type": "DRUG" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Echocardiography Test", "type": "PROCEDURE" }, { "name": "Gemcitabine", "type": "DRUG" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Multigated Acquisition Scan", "type": "PROCEDURE" }, { "name": "Pegylated Liposomal Doxorubicin Hydrochloride", "type": "DRUG" }, { "name": "Sacituzumab Govitecan", "type": "BIOLOGICAL" } ], "intervention_types": [ "BIOLOGICAL", "PROCEDURE", "DRUG" ], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 87, "start_date": "2026-09-24", "completion_date": "2029-04-12", "has_results": false, "last_update_posted_date": "2026-10-05", "last_synced_at": "2026-10-10T02:16:21.540Z", "location_count": 9, "location_summary": "Fayetteville, Arkansas • Rogers, Arkansas • Springdale, Arkansas + 6 more", "locations": [ { "city": "Fayetteville", "state": "Arkansas" }, { "city": "Rogers", "state": "Arkansas" }, { "city": "Springdale", "state": "Arkansas" }, { "city": "Coeur d'Alene", "state": "Idaho" }, { "city": "Post Falls", "state": "Idaho" } ], "official_url": "https://clinicaltrials.gov/study/NCT07504588" }, { "nct_id": "NCT07431931", "title": "Optimizing Referral Pathways for Patients With Hematuria and Moderate-Severe Proteinuria", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Referral and Consultation", "Glomerulonephritis", "Hematuria", "Proteinuria", "Kidney Disease" ], "interventions": [ { "name": "Electronic Health Record alert", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Geisinger Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1200, "start_date": "2026-11", "completion_date": "2027-12", "has_results": false, "last_update_posted_date": "2026-05-12", "last_synced_at": "2026-10-10T02:16:21.540Z", "location_count": 1, "location_summary": "Danville, Pennsylvania", "locations": [ { "city": "Danville", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT07431931" }, { "nct_id": "NCT04613362", "title": "TelemEdiciNe-bAsed Cognitive TherapY for Migraines", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Migraine Headache" ], "interventions": [ { "name": "TENACITY Telehealth Cognitive Behavioral Therapy for Migraine", "type": "BEHAVIORAL" }, { "name": "Behavioral Usual Care", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 80, "start_date": "2021-04-22", "completion_date": "2023-05-31", "has_results": true, "last_update_posted_date": "2024-09-19", "last_synced_at": "2026-10-10T02:16:21.540Z", "location_count": 4, "location_summary": "Birmingham, Alabama • West Haven, Connecticut • Indianapolis, Indiana + 1 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "West Haven", "state": "Connecticut" }, { "city": "Indianapolis", "state": "Indiana" }, { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04613362" }, { "nct_id": "NCT02312570", "title": "A Prospective, Randomized Clinical Trial of PRP Concepts Fibrin Bio-Matrix in Chronic Non-Healing Pressure Ulcers", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pressure Ulcer" ], "interventions": [ { "name": "PRP Concepts Fibrin Bio-Matrix", "type": "DEVICE" }, { "name": "Usual and Customary Practice", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "PRP Concepts, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 200, "start_date": "2021-01-01", "completion_date": "2021-12-31", "has_results": false, "last_update_posted_date": "2021-04-13", "last_synced_at": "2026-10-10T02:16:21.540Z", "location_count": 1, "location_summary": "Miami, Florida", "locations": [ { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02312570" }, { "nct_id": "NCT02970656", "title": "A Pilot Study of Biomarkers of Stress in Youth Who Use Teens.Connect", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetes Mellitus, Type 1" ], "interventions": [ { "name": "Teens.Connect", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "11 Years", "maximum_age": "14 Years", "sex": "ALL", "summary": "11 Years to 14 Years" }, "enrollment_count": 29, "start_date": "2017-02-08", "completion_date": "2019-02-28", "has_results": false, "last_update_posted_date": "2019-04-02", "last_synced_at": "2026-10-10T02:16:21.540Z", "location_count": 1, "location_summary": "West Haven, Connecticut", "locations": [ { "city": "West Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT02970656" }, { "nct_id": "NCT05793151", "title": "Multi-Site Trial of Navigation vs Treatment as Usual to Improve Initiation of Timely Adjuvant Therapy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Head and Neck Cancer", "Head and Neck Squamous Cell Carcinoma", "Oropharynx Cancer", "Oral Cavity Cancer", "Larynx Cancer" ], "interventions": [ { "name": "ENDURE", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Medical University of South Carolina", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 532, "start_date": "2023-10-30", "completion_date": "2028-03-30", "has_results": false, "last_update_posted_date": "2025-12-11", "last_synced_at": "2026-10-10T02:16:21.540Z", "location_count": 4, "location_summary": "St Louis, Missouri • Durham, North Carolina • Charleston, South Carolina + 1 more", "locations": [ { "city": "St Louis", "state": "Missouri" }, { "city": "Durham", "state": "North Carolina" }, { "city": "Charleston", "state": "South Carolina" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05793151" }, { "nct_id": "NCT03748173", "title": "Infasurf®(Calfactant) Aerosol for Infants With Bronchiolitis-AERO-04", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Bronchiolitis" ], "interventions": [ { "name": "Aerosolized Infasurf", "type": "COMBINATION_PRODUCT" } ], "intervention_types": [ "COMBINATION_PRODUCT" ], "sponsor": "ONY", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "0 Months", "maximum_age": "4 Months", "sex": "ALL", "summary": "0 Months to 4 Months" }, "enrollment_count": 13, "start_date": "2019-01-12", "completion_date": "2020-10-21", "has_results": false, "last_update_posted_date": "2020-10-23", "last_synced_at": "2026-10-10T02:16:21.540Z", "location_count": 1, "location_summary": "Richmond, Virginia", "locations": [ { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT03748173" } ] }