{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=ONE&page=64", "query": { "intervention": "ONE", "page": 64 }, "page_size": 10 }, "pagination": { "page": 64, "page_size": 10, "total_count": 2136, "total_pages": 214, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=ONE&page=65&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=ONE&page=63&page_size=10" }, "source": "local", "last_synced_at": "2026-11-04T00:57:04.425Z", "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": "NCT07170202", "title": "The Increasing Mindfulness Engagement Project", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acceptability", "Feasibility Studies", "Healthy Participants" ], "interventions": [ { "name": "Mindfulness Smartphone Application", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Florida State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "29 Years", "sex": "ALL", "summary": "18 Years to 29 Years" }, "enrollment_count": 40, "start_date": "2025-09-30", "completion_date": "2027-08-06", "has_results": false, "last_update_posted_date": "2026-07-13", "last_synced_at": "2026-10-20T14:16:21.795Z", "location_count": 1, "location_summary": "Tallahassee, Florida", "locations": [ { "city": "Tallahassee", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT07170202" }, { "nct_id": "NCT07051655", "title": "The Effects of Exogenous Ketones on Cognitive Function", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Ketone Monoester", "Placebo - Control" ], "interventions": [ { "name": "Ketone Monoester (KE)", "type": "DIETARY_SUPPLEMENT" }, { "name": "Placebo", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "University of Alabama at Birmingham", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "19 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "19 Years to 55 Years" }, "enrollment_count": 45, "start_date": "2025-12-01", "completion_date": "2027-07-31", "has_results": false, "last_update_posted_date": "2026-07-13", "last_synced_at": "2026-07-30T05:08:55.399Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT07051655" }, { "nct_id": "NCT06785129", "title": "Endometriosis and Migraine", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Endometriosis", "Migraine" ], "interventions": [ { "name": "Conditioned pain modulation (CPM) response", "type": "BEHAVIORAL" }, { "name": "Hormonal assessment", "type": "BIOLOGICAL" }, { "name": "Pain ratings", "type": "BEHAVIORAL" }, { "name": "Pressure stimuli", "type": "DEVICE" }, { "name": "Thermal stimuli", "type": "DEVICE" } ], "intervention_types": [ "BEHAVIORAL", "BIOLOGICAL", "DEVICE" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "12 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "12 Years to 45 Years · Female only" }, "enrollment_count": 120, "start_date": "2025-02-12", "completion_date": "2030-01-01", "has_results": false, "last_update_posted_date": "2026-07-13", "last_synced_at": "2026-08-15T08:19:58.263Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT06785129" }, { "nct_id": "NCT05654012", "title": "Migraine in Adolescents", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Migraine" ], "interventions": [ { "name": "Conditioned pain modulation (CPM) efficiency", "type": "BEHAVIORAL" }, { "name": "Hormonal assessment", "type": "DIAGNOSTIC_TEST" }, { "name": "MRI", "type": "DEVICE" }, { "name": "Migraine-related measures", "type": "BEHAVIORAL" }, { "name": "Neural assessments", "type": "BEHAVIORAL" }, { "name": "Pain ratings", "type": "BEHAVIORAL" }, { "name": "Pressure pain thresholds (PPT)", "type": "BEHAVIORAL" }, { "name": "Pressure stimuli", "type": "DEVICE" }, { "name": "Pubertal status", "type": "DIAGNOSTIC_TEST" }, { "name": "Thermal Stimuli", "type": "DEVICE" } ], "intervention_types": [ "BEHAVIORAL", "DIAGNOSTIC_TEST", "DEVICE" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "10 Years", "maximum_age": "13 Years", "sex": "ALL", "summary": "10 Years to 13 Years" }, "enrollment_count": 250, "start_date": "2023-06-01", "completion_date": "2030-03-15", "has_results": false, "last_update_posted_date": "2026-07-13", "last_synced_at": "2026-07-29T01:19:57.199Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT05654012" }, { "nct_id": "NCT04783857", "title": "Modifying Progesterone and Estradiol Levels to Prevent Postpartum Cigarette Smoking Relapse and Reduce Secondhand Smoke Exposure in Infants and Children", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Smoking", "Smoking Cessation", "Smoking Reduction" ], "interventions": [ { "name": "Progesterone 200 MG Oral Capsule", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Minnesota", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "18 Years to 45 Years · Female only" }, "enrollment_count": 171, "start_date": "2022-04-14", "completion_date": "2027-06-02", "has_results": false, "last_update_posted_date": "2026-07-13", "last_synced_at": "2026-08-02T01:03:43.545Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT04783857" }, { "nct_id": "NCT02604563", "title": "Aging, Geriatric Syndromes and Clonal Hematopoiesis", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Aged", "Cardiovascular Diseases", "Geriatric Syndromes", "Geriatrics" ], "interventions": [ { "name": "Activities of Daily Living Questionnaire", "type": "OTHER" }, { "name": "Blood draw for trauma measurements", "type": "PROCEDURE" }, { "name": "Blood pressure measurement", "type": "OTHER" }, { "name": "Bone marrow aspirate", "type": "OTHER" }, { "name": "Buccal Swab", "type": "GENETIC" }, { "name": "Cognitive Assessment", "type": "OTHER" }, { "name": "Femur head donation", "type": "OTHER" }, { "name": "Gait Speed", "type": "OTHER" }, { "name": "Grip Strength", "type": "OTHER" }, { "name": "Heart Health and Smoking History from BRFSS questionnaire", "type": "OTHER" }, { "name": "Height and Weight measurements", "type": "OTHER" }, { "name": "Instrumental Activities of Daily Living, subscale of the OARS", "type": "OTHER" }, { "name": "Karnofsky Self-reported Performance Rating Scale", "type": "OTHER" }, { "name": "Knee bone fragments", "type": "OTHER" }, { "name": "MOS Social Activity Survey", "type": "OTHER" }, { "name": "Number of Falls", "type": "OTHER" }, { "name": "Optional bone marrow biopsy", "type": "PROCEDURE" }, { "name": "Peripheral Blood Draw", "type": "GENETIC" }, { "name": "Physical Health Section, subscale of the OARS", "type": "OTHER" }, { "name": "Unintentional Weight Loss", "type": "OTHER" } ], "intervention_types": [ "OTHER", "PROCEDURE", "GENETIC" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 2000, "start_date": "2016-03-10", "completion_date": "2030-04-30", "has_results": false, "last_update_posted_date": "2026-07-13", "last_synced_at": "2026-10-14T18:19:26.684Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT02604563" }, { "nct_id": "NCT06967545", "title": "A One-Arm Open Trial of a Smartphone Delivered Treatment for Suicidal Thoughts and Behavior", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Suicide Attempt", "Suicide Ideation" ], "interventions": [ { "name": "Smartphone-delivered Therapeutic Evaluative Conditioning for Suicide (TEC-S)", "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": 20, "start_date": "2026-01-20", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-07-10", "last_synced_at": "2026-08-01T12:53:13.848Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT06967545" }, { "nct_id": "NCT06628687", "title": "A Study to Learn How BIIB141 (Omaveloxolone) Affects the Health of Participants With Friedrich's Ataxia Who Took it During Pregnancy and/or During Breastfeeding and About the Health of Their Babies", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Friedreich Ataxia" ], "interventions": [ { "name": "Omaveloxolone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Biogen", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "16 Years", "maximum_age": null, "sex": "FEMALE", "summary": "16 Years and older · Female only" }, "enrollment_count": 10, "start_date": "2026-10-26", "completion_date": "2035-04-30", "has_results": false, "last_update_posted_date": "2026-07-10", "last_synced_at": "2026-07-30T03:53:08.356Z", "location_count": 1, "location_summary": "Morrisville, North Carolina", "locations": [ { "city": "Morrisville", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06628687" }, { "nct_id": "NCT06033950", "title": "A Study to Evaluate Finerenone on Clinical Efficacy and Safety in Patients With Heart Failure Who Are Intolerant or Not Eligible for Treatment With Steroidal Mineralocorticoid Receptor Antagonists", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Heart Failure" ], "interventions": [ { "name": "Finerenone", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Colorado Prevention Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 2600, "start_date": "2024-08-20", "completion_date": "2028-01", "has_results": false, "last_update_posted_date": "2026-07-10", "last_synced_at": "2026-11-04T00:57:04.425Z", "location_count": 54, "location_summary": "Fairhope, Alabama • Phoenix, Arizona • Yuma, Arizona + 45 more", "locations": [ { "city": "Fairhope", "state": "Alabama" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Yuma", "state": "Arizona" }, { "city": "Chula Vista", "state": "California" }, { "city": "Chula Vista", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06033950" }, { "nct_id": "NCT03593759", "title": "Cardiac Sarcoidosis Randomized Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Cardiac Sarcoidosis", "Sarcoidosis" ], "interventions": [ { "name": "Methotrexate", "type": "DRUG" }, { "name": "Prednisone or Prednisolone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Ottawa Heart Institute Research Corporation", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 160, "start_date": "2019-01-15", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2026-07-10", "last_synced_at": "2026-10-14T20:48:39.070Z", "location_count": 9, "location_summary": "New Haven, Connecticut • Boston, Massachusetts • Ann Arbor, Michigan + 6 more", "locations": [ { "city": "New Haven", "state": "Connecticut" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "Ann Arbor", "state": "Michigan" }, { "city": "Minneota", "state": "Minnesota" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03593759" } ] }