{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?healthyVolunteers=true&page=44&status=RECRUITING", "query": { "status": "RECRUITING", "healthyVolunteers": true, "page": 44 }, "page_size": 10 }, "pagination": { "page": 44, "page_size": 10, "total_count": 5029, "total_pages": 503, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?healthyVolunteers=true&page=45&status=RECRUITING&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?healthyVolunteers=true&page=43&status=RECRUITING&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-16T00:31:29.611Z", "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": "NCT07117669", "title": "Study of ENP-501 in Peanut-Allergic and Non-Allergic Participants", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Peanut Allergy" ], "interventions": [ { "name": "ENP-501", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "N-Fold, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "14 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "14 Years to 50 Years" }, "enrollment_count": 68, "start_date": "2025-12-16", "completion_date": "2028-11", "has_results": false, "last_update_posted_date": "2026-04-24", "last_synced_at": "2026-10-16T00:31:29.611Z", "location_count": 1, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT07117669" }, { "nct_id": "NCT07586982", "title": "Clinical Performance of Verofilcon A Toric Contact Lenses", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Contact Lenses", "Presbyopia" ], "interventions": [ { "name": "Total 30 multi foric contact lenses", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Southern College of Optometry", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "ALL", "summary": "18 Years to 40 Years" }, "enrollment_count": 32, "start_date": "2026-04", "completion_date": "2026-09", "has_results": false, "last_update_posted_date": "2026-05-14", "last_synced_at": "2026-10-16T00:31:29.611Z", "location_count": 1, "location_summary": "Memphis, Tennessee", "locations": [ { "city": "Memphis", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT07586982" }, { "nct_id": "NCT06315582", "title": "Surgical Approach to Uterine Septum", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Uterine Septum", "Surgical Complication", "Septum; Uterus", "Treatment Side Effects", "Treatment" ], "interventions": [ { "name": "Removal of uterine septum with hysteroscopic scissors without electrosurgery.", "type": "PROCEDURE" }, { "name": "Hysteroscopic septoplasty utilizing bipolar electrosurgery", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "22 Years", "maximum_age": "44 Years", "sex": "FEMALE", "summary": "22 Years to 44 Years · Female only" }, "enrollment_count": 40, "start_date": "2024-03-11", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2026-06-01", "last_synced_at": "2026-10-16T00:31:29.611Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06315582" }, { "nct_id": "NCT06922188", "title": "Development of Measures to Screen for Financial Hardship in Alzheimer's Disease and Dementia", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Financial Hardship", "Alzheimer's Disease (AD)", "Alzheimer's Disease and Related Dementia (ADRD)" ], "interventions": [], "intervention_types": [], "sponsor": "Fred Hutchinson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 2460, "start_date": "2025-03-31", "completion_date": "2029-12-18", "has_results": false, "last_update_posted_date": "2026-08-19", "last_synced_at": "2026-10-16T00:31:29.611Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT06922188" }, { "nct_id": "NCT06033703", "title": "Topical Netarsudil for the Prevention of Proliferative Vitreoretinopathy in Patients With Retinal Detachment", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Rhegmatogenous Retinal Detachment", "Proliferative Vitreoretinopathy" ], "interventions": [ { "name": "Netarsudil Ophthalmic", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Massachusetts Eye and Ear Infirmary", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 48, "start_date": "2025-01-14", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2025-10-28", "last_synced_at": "2026-10-16T00:31:29.611Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT06033703" }, { "nct_id": "NCT06798571", "title": "Role of Menopause in Thermoregulation", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Menopause", "Aging" ], "interventions": [ { "name": "Elagolix Oral Tablet", "type": "DRUG" }, { "name": "Estradiol patch", "type": "DRUG" }, { "name": "cellulose placebo", "type": "OTHER" }, { "name": "placebo patch", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Penn State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "42 Years", "maximum_age": "64 Years", "sex": "FEMALE", "summary": "42 Years to 64 Years · Female only" }, "enrollment_count": 24, "start_date": "2025-03-01", "completion_date": "2026-12-01", "has_results": false, "last_update_posted_date": "2026-10-02", "last_synced_at": "2026-10-16T00:31:29.611Z", "location_count": 1, "location_summary": "University Park, Pennsylvania", "locations": [ { "city": "University Park", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06798571" }, { "nct_id": "NCT06613204", "title": "STELLA-FTD: Examination of a Behavior Change Intervention for FTD Family Care Partners", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Frontotemporal Dementia", "Caregiver Burden", "Primary Progressive Aphasia (PPA)", "Corticobasal Syndrome" ], "interventions": [ { "name": "STELLA-FTD Control", "type": "BEHAVIORAL" }, { "name": "STELLA-FTD Test", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Oregon Health and Science University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 640, "start_date": "2025-06-23", "completion_date": "2029-06", "has_results": false, "last_update_posted_date": "2025-10-27", "last_synced_at": "2026-10-16T00:31:29.611Z", "location_count": 1, "location_summary": "Portland, Oregon", "locations": [ { "city": "Portland", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT06613204" }, { "nct_id": "NCT07063732", "title": "Ketone Monoester Supplements, High Altitude, and Brain Blood Flow During Exercise", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "High Altitude Hypoxia", "Exercise" ], "interventions": [ { "name": "Ketone Monoester (KME)", "type": "DIETARY_SUPPLEMENT" }, { "name": "Placebo", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "McMaster University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "35 Years", "sex": "ALL", "summary": "18 Years to 35 Years" }, "enrollment_count": 14, "start_date": "2025-05-28", "completion_date": "2025-08-31", "has_results": false, "last_update_posted_date": "2025-07-14", "last_synced_at": "2026-10-16T00:31:29.611Z", "location_count": 1, "location_summary": "Bishop, California", "locations": [ { "city": "Bishop", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT07063732" }, { "nct_id": "NCT04331704", "title": "ANCHORS Alcohol & Sexual Health Study: UH3 Project", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Alcohol Use, Unspecified", "Substance Use", "Sex Behavior" ], "interventions": [ { "name": "PrEP acronym (pre-exposure prophylaxis)", "type": "DRUG" }, { "name": "Initial Web Survey", "type": "BEHAVIORAL" }, { "name": "Interactive Voice Response (IVR) monitoring", "type": "BEHAVIORAL" }, { "name": "Educational material on alcohol and sexual health behavior", "type": "BEHAVIORAL" }, { "name": "Interactive Voice Response (IVR) assessment with personalized information", "type": "BEHAVIORAL" }, { "name": "Personalized information based on web-based survey responses & standardized information", "type": "BEHAVIORAL" } ], "intervention_types": [ "DRUG", "BEHAVIORAL" ], "sponsor": "University of Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "30 Years", "sex": "MALE", "summary": "18 Years to 30 Years · Male only" }, "enrollment_count": 88, "start_date": "2021-01-12", "completion_date": "2026-06-30", "has_results": false, "last_update_posted_date": "2025-07-10", "last_synced_at": "2026-10-16T00:31:29.611Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT04331704" }, { "nct_id": "NCT03892993", "title": "Patient Decision Aid in Supporting Decision-Making About When to Start or Stop New Drugs, Join Clinical Trials, or Continue Active Surveillance in Patients With Medullary Thyroid Cancer and Their Caregivers", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Thyroid Gland Medullary Carcinoma" ], "interventions": [ { "name": "Decision Aid", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "M.D. Anderson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2019-04-09", "completion_date": "2028-08-01", "has_results": false, "last_update_posted_date": "2026-07-16", "last_synced_at": "2026-10-16T00:31:29.611Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03892993" } ] }