{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=CORTEX&page=4", "query": { "intervention": "CORTEX", "page": 4 }, "page_size": 10 }, "pagination": { "page": 4, "page_size": 10, "total_count": 1865, "total_pages": 187, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=CORTEX&page=5&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=CORTEX&page=3&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-21T21:04:59.362Z", "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": "NCT07659691", "title": "Multisensory Rehabilitation of Vision Loss After Cortical Damage", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cortical Blindness" ], "interventions": [ { "name": "Multisensory Rehabilitation", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 30, "start_date": "2026-10", "completion_date": "2027-12", "has_results": false, "last_update_posted_date": "2026-08-27", "last_synced_at": "2026-10-21T21:04:59.362Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT07659691" }, { "nct_id": "NCT06317662", "title": "Testing the Addition of the Anti-cancer Drug Venetoclax and/or the Anti-cancer Immunotherapy Blinatumomab to the Usual Chemotherapy Treatment for Infants With Newly Diagnosed KMT2A-rearranged or KMT2A-non-rearranged Leukemia", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Acute Leukemia of Ambiguous Lineage", "B Acute Lymphoblastic Leukemia" ], "interventions": [ { "name": "Asparaginase Erwinia chrysanthemi", "type": "DRUG" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Blinatumomab", "type": "BIOLOGICAL" }, { "name": "Bone Marrow Aspiration", "type": "PROCEDURE" }, { "name": "Calaspargase Pegol", "type": "DRUG" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Cyclophosphamide", "type": "DRUG" }, { "name": "Cytarabine", "type": "DRUG" }, { "name": "Daunorubicin", "type": "DRUG" }, { "name": "Dexamethasone", "type": "DRUG" }, { "name": "Doxorubicin", "type": "DRUG" }, { "name": "Echocardiography Test", "type": "PROCEDURE" }, { "name": "FDG-Positron Emission Tomography", "type": "PROCEDURE" }, { "name": "Leucovorin", "type": "DRUG" }, { "name": "Levoleucovorin", "type": "DRUG" }, { "name": "Lumbar Puncture", "type": "PROCEDURE" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Mercaptopurine", "type": "DRUG" }, { "name": "Methotrexate", "type": "DRUG" }, { "name": "Methylprednisolone", "type": "DRUG" }, { "name": "Multigated Acquisition Scan", "type": "PROCEDURE" }, { "name": "Prednisolone", "type": "DRUG" }, { "name": "Prednisone", "type": "DRUG" }, { "name": "Therapeutic Hydrocortisone", "type": "DRUG" }, { "name": "Thioguanine", "type": "DRUG" }, { "name": "Venetoclax", "type": "DRUG" }, { "name": "Vincristine", "type": "DRUG" } ], "intervention_types": [ "DRUG", "PROCEDURE", "BIOLOGICAL" ], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "365 Days", "sex": "ALL", "summary": "Up to 365 Days" }, "enrollment_count": 153, "start_date": "2025-06-05", "completion_date": "2028-12-31", "has_results": false, "last_update_posted_date": "2026-10-21", "last_synced_at": "2026-10-21T21:04:59.362Z", "location_count": 116, "location_summary": "Birmingham, Alabama • Anchorage, Alaska • Mesa, Arizona + 100 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Anchorage", "state": "Alaska" }, { "city": "Mesa", "state": "Arizona" }, { "city": "Little Rock", "state": "Arkansas" }, { "city": "Loma Linda", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06317662" }, { "nct_id": "NCT04170803", "title": "Feasibility of Near-infrared Spectroscopy to Measure Cortical Pain Pathway (Brain) Activation During Dry Needling", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Shoulder Pain", "Chronic Pain", "Musculoskeletal Injury" ], "interventions": [ { "name": "Dry Needling", "type": "DEVICE" }, { "name": "Sham Dry Needling", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Army-Baylor University Doctoral Program in Physical Therapy", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "18 Years to 50 Years" }, "enrollment_count": 18, "start_date": "2019-01-08", "completion_date": "2020-07-24", "has_results": false, "last_update_posted_date": "2020-07-28", "last_synced_at": "2026-10-21T21:04:59.362Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04170803" }, { "nct_id": "NCT02126124", "title": "Evaluation of Deep Transcranial Magnetic Stimulation (DTMS) With the H-ADD Coil as an Aid to Smoking Cessation.", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Smoking Cessation" ], "interventions": [ { "name": "Sham Treatment", "type": "DEVICE" }, { "name": "Active dTMS Treatment", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Brainsway", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "22 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "22 Years to 70 Years" }, "enrollment_count": 224, "start_date": "2014-08-20", "completion_date": "2019-11-14", "has_results": false, "last_update_posted_date": "2020-12-04", "last_synced_at": "2026-10-21T21:04:59.362Z", "location_count": 14, "location_summary": "Los Angeles, California • San Diego, California • Denver, Colorado + 10 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "San Diego", "state": "California" }, { "city": "Denver", "state": "Colorado" }, { "city": "Gainesville", "state": "Florida" }, { "city": "Juno Beach", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02126124" }, { "nct_id": "NCT00927173", "title": "Evaluation of the Brainsway Deep Transcranial Magnetic Stimulation (TMS) H-Coil in the Treatment of Major Depression Disorder", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Major Depressive Disorder" ], "interventions": [ { "name": "Brainsway H-Coil Deep TMS System", "type": "DEVICE" }, { "name": "Brainsway H-Coil Deep TMS System (Sham treatment)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Brainsway", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": "68 Years", "sex": "ALL", "summary": "22 Years to 68 Years" }, "enrollment_count": 233, "start_date": "2009-09", "completion_date": "2012-06", "has_results": false, "last_update_posted_date": "2020-07-15", "last_synced_at": "2026-10-21T21:04:59.362Z", "location_count": 14, "location_summary": "Los Angeles, California • Sacramento and Davis, California • Santa Monica, California + 10 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Sacramento and Davis", "state": "California" }, { "city": "Santa Monica", "state": "California" }, { "city": "Juno Beach", "state": "Florida" }, { "city": "Royal Palm Beach", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT00927173" }, { "nct_id": "NCT01567982", "title": "Effects of Transcranial Direct Current Stimulation on Tobacco Withdrawal Symptoms", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Nicotine Withdrawal", "Tobacco Abstinence" ], "interventions": [ { "name": "tDCS, prefrontal cortex and parietal cortex", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "18 Years to 55 Years" }, "enrollment_count": 60, "start_date": "2011-03", "completion_date": "2015-07", "has_results": false, "last_update_posted_date": "2015-07-15", "last_synced_at": "2026-10-21T21:04:59.362Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT01567982" }, { "nct_id": "NCT05074524", "title": "Repetitive Transcranial Magnetic Stimulation to Reduce Heroin Cravings", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Opioid-use Disorder", "Heroin Abuse", "Craving", "Transcranial Magnetic Stimulation" ], "interventions": [ { "name": "Repetitive Transcranial Magnetic Stimulation", "type": "DEVICE" }, { "name": "Sham Repetitive Transcranial Magnetic Stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Nevada, Las Vegas", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "18 Years to 64 Years" }, "enrollment_count": 24, "start_date": "2021-10-06", "completion_date": "2022-01-24", "has_results": false, "last_update_posted_date": "2022-05-17", "last_synced_at": "2026-10-21T21:04:59.362Z", "location_count": 1, "location_summary": "Las Vegas, Nevada", "locations": [ { "city": "Las Vegas", "state": "Nevada" } ], "official_url": "https://clinicaltrials.gov/study/NCT05074524" }, { "nct_id": "NCT03891888", "title": "Intramedullary Bone Grafting for Open Tibial Shaft Fractures", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Tibial Fractures", "Nonunion of Fracture", "Delayed Union of Fracture" ], "interventions": [ { "name": "Intramedullary Bone Graft", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of Louisville", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 130, "start_date": "2020-03-26", "completion_date": "2025-02", "has_results": false, "last_update_posted_date": "2024-05-22", "last_synced_at": "2026-10-21T21:04:59.362Z", "location_count": 1, "location_summary": "Louisville, Kentucky", "locations": [ { "city": "Louisville", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT03891888" }, { "nct_id": "NCT02909686", "title": "Effects of Botanical Microglia Modulators in Gulf War Illness", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Gulf War Illness" ], "interventions": [ { "name": "Boswellia Serrata", "type": "DIETARY_SUPPLEMENT" }, { "name": "Curcumin", "type": "DIETARY_SUPPLEMENT" }, { "name": "Epimedium", "type": "DIETARY_SUPPLEMENT" }, { "name": "Fisetin", "type": "DIETARY_SUPPLEMENT" }, { "name": "Luteolin", "type": "DIETARY_SUPPLEMENT" }, { "name": "Nettle", "type": "DIETARY_SUPPLEMENT" }, { "name": "Pycnogenol", "type": "DIETARY_SUPPLEMENT" }, { "name": "Reishi Mushroom", "type": "DIETARY_SUPPLEMENT" }, { "name": "Resveratrol", "type": "DIETARY_SUPPLEMENT" }, { "name": "Placebo", "type": "DIETARY_SUPPLEMENT" } ], "intervention_types": [ "DIETARY_SUPPLEMENT" ], "sponsor": "University of Alabama at Birmingham", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "39 Years", "maximum_age": "65 Years", "sex": "MALE", "summary": "39 Years to 65 Years · Male only" }, "enrollment_count": 36, "start_date": "2016-07", "completion_date": "2022-09", "has_results": true, "last_update_posted_date": "2025-01-24", "last_synced_at": "2026-10-21T21:04:59.362Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT02909686" }, { "nct_id": "NCT02410382", "title": "Dexamethasone for Treatment of Radiation-related Fatigue in Patients Receiving RT for Head-neck and Lung Cancer", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Head and Neck Cancer", "Non-small Cell Lung Cancer" ], "interventions": [ { "name": "Dexamethasone", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Arizona", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 79, "start_date": "2014-08-27", "completion_date": "2018-02-16", "has_results": true, "last_update_posted_date": "2019-05-14", "last_synced_at": "2026-10-21T21:04:59.362Z", "location_count": 1, "location_summary": "Tucson, Arizona", "locations": [ { "city": "Tucson", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT02410382" } ] }