{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=PRE&page=39", "query": { "intervention": "PRE", "page": 39 }, "page_size": 10 }, "pagination": { "page": 39, "page_size": 10, "total_count": 1548, "total_pages": 155, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=PRE&page=40&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=PRE&page=38&page_size=10" }, "source": "local", "last_synced_at": "2026-10-15T03:55:53.102Z", "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": "NCT05450718", "title": "Low-dose Buprenorphine Initiation for Opioid Use Disorder", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Opioid Use Disorder" ], "interventions": [ { "name": "buprenorphine-naloxone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Montefiore 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": 70, "start_date": "2024-11-11", "completion_date": "2027-06-30", "has_results": false, "last_update_posted_date": "2026-07-21", "last_synced_at": "2026-07-26T20:59:25.636Z", "location_count": 1, "location_summary": "The Bronx, New York", "locations": [ { "city": "The Bronx", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05450718" }, { "nct_id": "NCT07607470", "title": "Large Algorithm Setting and Validation Study", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Bacterial Infections", "Bacterial Infections and Mycoses", "Candidiasis", "Female Urogenital Diseases", "Genital Diseases, Female", "Infections", "Mycoses", "Urogenital Disease", "Vaginal Diseases", "Vaginitis", "Vaginosis, Bacterial", "Vulvar Diseases", "Vulvovaginitis" ], "interventions": [ { "name": "BD Max™ Vaginal Panel", "type": "DIAGNOSTIC_TEST" }, { "name": "Cepheid Xpert® Xpress MVP", "type": "DIAGNOSTIC_TEST" }, { "name": "Hologic Aptima® BV Assay", "type": "DIAGNOSTIC_TEST" }, { "name": "Nanopath Vaginitis Assay", "type": "DIAGNOSTIC_TEST" }, { "name": "Yeast Culture", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Nanopath, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 1000, "start_date": "2026-06-03", "completion_date": "2027-01", "has_results": false, "last_update_posted_date": "2026-07-20", "last_synced_at": "2026-07-28T03:10:19.127Z", "location_count": 2, "location_summary": "North Miami, Florida • New Orleans, Louisiana", "locations": [ { "city": "North Miami", "state": "Florida" }, { "city": "New Orleans", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT07607470" }, { "nct_id": "NCT07401940", "title": "HAVEN-Connect Youth Suicide Prevention", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Suicide Prevention" ], "interventions": [ { "name": "HAVEN Suicide Prevention", "type": "BEHAVIORAL" }, { "name": "HAVEN-Connect", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "George Washington University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "13 Years", "maximum_age": "19 Years", "sex": "ALL", "summary": "13 Years to 19 Years" }, "enrollment_count": 240, "start_date": "2023-06-01", "completion_date": "2026-11-30", "has_results": false, "last_update_posted_date": "2026-07-20", "last_synced_at": "2026-08-01T23:56:06.470Z", "location_count": 2, "location_summary": "New York, New York • Rochester, New York", "locations": [ { "city": "New York", "state": "New York" }, { "city": "Rochester", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07401940" }, { "nct_id": "NCT07185204", "title": "Postpartum Preeclampsia Early Detection and Treatment: Nepal Pilot Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postpartum Preeclampsia" ], "interventions": [ { "name": "Early detection and management of postpartum preeclampsia bundle", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Medical College of Wisconsin", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 60, "start_date": "2026-03-03", "completion_date": "2027-06", "has_results": false, "last_update_posted_date": "2026-07-20", "last_synced_at": "2026-07-30T10:44:16.540Z", "location_count": 1, "location_summary": "Milwaukee, Wisconsin", "locations": [ { "city": "Milwaukee", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT07185204" }, { "nct_id": "NCT07136948", "title": "Mindfulness Training and Respiration Biosignal Feedback - Study 2", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mindfulness Skills", "Psychological Distress", "Usability Satisfaction" ], "interventions": [ { "name": "Mindfulness Meditation", "type": "BEHAVIORAL" }, { "name": "Mindfulness Meditation with Respiration Feedback Chart and Predictive Mindfulness Skill Scores", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Equa Health", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "30 Years", "sex": "ALL", "summary": "18 Years to 30 Years" }, "enrollment_count": 60, "start_date": "2025-07-21", "completion_date": "2026-09", "has_results": false, "last_update_posted_date": "2026-07-20", "last_synced_at": "2026-07-30T08:51:23.873Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT07136948" }, { "nct_id": "NCT06378866", "title": "Stereotactic Body Radiation Therapy Plus Immediate or Delayed Androgen Receptor Pathway Inhibitor and Androgen Deprivation Therapy or Salvage Radiation Therapy for the Treatment of Prostate Cancer, DIVINE Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Biochemically Recurrent Prostate Carcinoma", "Castration-resistant Prostate Cancer", "Recurrent Castration-Sensitive Prostate Carcinoma", "Recurrent Prostate Cancer" ], "interventions": [ { "name": "Abiraterone", "type": "DRUG" }, { "name": "Apalutamide", "type": "DRUG" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Bone Scan", "type": "PROCEDURE" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Darolutamide", "type": "DRUG" }, { "name": "Degarelix", "type": "DRUG" }, { "name": "Enzalutamide", "type": "DRUG" }, { "name": "Goserelin", "type": "DRUG" }, { "name": "Histrelin", "type": "DRUG" }, { "name": "Image-Guided Therapy", "type": "PROCEDURE" }, { "name": "Leuprolide", "type": "DRUG" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Patient Observation", "type": "OTHER" }, { "name": "Positron Emission Tomography", "type": "PROCEDURE" }, { "name": "Prednisone", "type": "DRUG" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Radiation Therapy", "type": "RADIATION" }, { "name": "Relugolix", "type": "DRUG" }, { "name": "Stereotactic Body Radiation Therapy", "type": "RADIATION" }, { "name": "Triptorelin", "type": "DRUG" } ], "intervention_types": [ "DRUG", "PROCEDURE", "OTHER", "RADIATION" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 532, "start_date": "2024-06-03", "completion_date": "2031-02-28", "has_results": false, "last_update_posted_date": "2026-07-20", "last_synced_at": "2026-10-15T03:55:53.102Z", "location_count": 3, "location_summary": "Phoenix, Arizona • Jacksonville, Florida • Rochester, Minnesota", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Jacksonville", "state": "Florida" }, { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT06378866" }, { "nct_id": "NCT06289010", "title": "Neural Mechanisms of Family-Focused Treatment for Youth Depression", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Childhood Depression" ], "interventions": [ { "name": "Family-Focused Treatment for Childhood-Depression (FFT-CD)", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Boston University Charles River Campus", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "7 Years", "maximum_age": "12 Years", "sex": "ALL", "summary": "7 Years to 12 Years" }, "enrollment_count": 80, "start_date": "2024-08-20", "completion_date": "2027-11", "has_results": false, "last_update_posted_date": "2026-07-20", "last_synced_at": "2026-07-27T10:40:29.890Z", "location_count": 2, "location_summary": "Boston, Massachusetts • Charlestown, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "Charlestown", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT06289010" }, { "nct_id": "NCT07708844", "title": "Structured Opportunities for Connection to Improve Aging-related Loneliness", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Loneliness" ], "interventions": [ { "name": "Prescribing of community activities; at least 2 hours per week", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Endeavor Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "55 Years", "maximum_age": null, "sex": "ALL", "summary": "55 Years and older" }, "enrollment_count": 50, "start_date": "2026-05-01", "completion_date": "2027-05-01", "has_results": false, "last_update_posted_date": "2026-07-17", "last_synced_at": "2026-08-04T04:07:35.390Z", "location_count": 1, "location_summary": "Evanston, Illinois", "locations": [ { "city": "Evanston", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT07708844" }, { "nct_id": "NCT07603739", "title": "Eating Almonds Before a Meal to Control Blood Sugar", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Glucose Control", "Nutrition", "Precision Medicine", "Prediabetes (Insulin Resistance, Impaired Glucose Tolerance)" ], "interventions": [ { "name": "Premeal almond ingestion", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "Pennington Biomedical Research Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "25 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "25 Years to 50 Years" }, "enrollment_count": 25, "start_date": "2026-06-23", "completion_date": "2028-07", "has_results": false, "last_update_posted_date": "2026-07-17", "last_synced_at": "2026-07-30T07:31:39.045Z", "location_count": 1, "location_summary": "Baton Rouge, Louisiana", "locations": [ { "city": "Baton Rouge", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT07603739" }, { "nct_id": "NCT07052344", "title": "Gut-Brain Neural Coupling in Spinal Cord Injury", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "SCI - Spinal Cord Injury" ], "interventions": [ { "name": "Ad-libitum control condition", "type": "OTHER" }, { "name": "Preload condition", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Miami", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 28, "start_date": "2025-10-29", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-07-17", "last_synced_at": "2026-07-26T20:25:50.622Z", "location_count": 1, "location_summary": "Miami, Florida", "locations": [ { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT07052344" } ] }