{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sham-Control&page=12", "query": { "intervention": "Sham-Control", "page": 12 }, "page_size": 10 }, "pagination": { "page": 12, "page_size": 10, "total_count": 1656, "total_pages": 166, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sham-Control&page=13&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sham-Control&page=11&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-23T15:31:11.328Z", "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": "NCT07202702", "title": "Modulation of Motor Learning Via tDCS in a Dexterous Video Game Task", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Motor Activity" ], "interventions": [ { "name": "tDCS", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "ALL", "summary": "18 Years to 45 Years" }, "enrollment_count": 40, "start_date": "2025-04-04", "completion_date": "2025-12-03", "has_results": true, "last_update_posted_date": "2026-10-22", "last_synced_at": "2026-10-23T15:31:11.328Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT07202702" }, { "nct_id": "NCT03261505", "title": "Mechanistic Studies on Video-guided Acupuncture Imagery Treatment of Knee Pain", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Osteoarthritis, Knee" ], "interventions": [ { "name": "Acupuncture", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "40 Years to 70 Years" }, "enrollment_count": 125, "start_date": "2019-08-04", "completion_date": "2023-08-31", "has_results": true, "last_update_posted_date": "2025-11-05", "last_synced_at": "2026-10-23T15:31:11.328Z", "location_count": 1, "location_summary": "Charlestown, Massachusetts", "locations": [ { "city": "Charlestown", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT03261505" }, { "nct_id": "NCT05637801", "title": "A Pivotal Study of Sensory Stimulation in Alzheimer's Disease (HOPE Study)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alzheimer Disease", "Alzheimer Disease 1", "Alzheimer Disease 2", "Alzheimer Disease 3", "Alzheimer Disease, Early Onset", "Alzheimer Disease, Late Onset", "Alzheimer Disease 9", "Alzheimer Disease 4", "Alzheimer Disease 7", "Alzheimer Disease 17", "Alzheimer's Dementia Late Onset", "Alzheimer Disease 5", "Alzheimer Disease 6", "Alzheimer Disease 8", "Alzheimer Disease 10", "Alzheimer Disease 11", "Alzheimer Disease 12", "Alzheimer Disease 13", "Alzheimer Disease 14", "Alzheimer Disease 15", "Alzheimer Disease 16", "Alzheimer Disease 18", "Alzheimer Disease 19", "Dementia", "Dementia Alzheimers", "Dementia, Mild", "Dementia of Alzheimer Type", "Dementia Moderate", "Dementia Senile", "Mild Cognitive Impairment", "Mild Dementia", "MCI", "Cognitive Impairment", "Cognitive Decline", "Cognitive Impairment, Mild" ], "interventions": [ { "name": "Spectris™ AD - Active", "type": "DEVICE" }, { "name": "Spectris™ AD - Sham", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Cognito Therapeutics, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "50 Years to 90 Years" }, "enrollment_count": 673, "start_date": "2022-12-13", "completion_date": "2026-08-17", "has_results": false, "last_update_posted_date": "2026-09-09", "last_synced_at": "2026-10-23T15:31:11.328Z", "location_count": 68, "location_summary": "Gilbert, Arizona • Phoenix, Arizona • Sun City, Arizona + 62 more", "locations": [ { "city": "Gilbert", "state": "Arizona" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Sun City", "state": "Arizona" }, { "city": "Anaheim", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05637801" }, { "nct_id": "NCT03244475", "title": "Transcranial Electrical Stimulation for mTBI", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mild Traumatic Brain Injury (mTBI)", "Post-traumatic Stress Disorder" ], "interventions": [ { "name": "TES", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 66, "start_date": "2017-02-01", "completion_date": "2022-09-30", "has_results": true, "last_update_posted_date": "2024-01-18", "last_synced_at": "2026-10-23T15:31:11.328Z", "location_count": 1, "location_summary": "San Diego, California", "locations": [ { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03244475" }, { "nct_id": "NCT03629275", "title": "Investigation of Neural Stem Cells in Ischemic Stroke", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Ischemic Stroke", "Chronic Stroke", "Hemiparesis", "Arm Paralysis" ], "interventions": [ { "name": "CTX0E03 Drug Product and delivery device", "type": "COMBINATION_PRODUCT" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "COMBINATION_PRODUCT", "DRUG" ], "sponsor": "ReNeuron Limited", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "35 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "35 Years to 75 Years" }, "enrollment_count": 15, "start_date": "2018-08-31", "completion_date": "2021-03-02", "has_results": false, "last_update_posted_date": "2021-08-13", "last_synced_at": "2026-10-23T15:31:11.328Z", "location_count": 23, "location_summary": "Little Rock, Arkansas • Irvine, California • Los Angeles, California + 19 more", "locations": [ { "city": "Little Rock", "state": "Arkansas" }, { "city": "Irvine", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Palo Alto", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03629275" }, { "nct_id": "NCT03882931", "title": "Functional Roles of Dorsolateral Prefrontal Cortex", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Healthy Participants" ], "interventions": [ { "name": "Theta Burst Transcranial Magnetic Stimulation", "type": "OTHER" }, { "name": "Focused Ultrasound", "type": "OTHER" }, { "name": "Sham", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Virginia", "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": 90, "start_date": "2019-01-28", "completion_date": "2020-01-27", "has_results": false, "last_update_posted_date": "2019-11-19", "last_synced_at": "2026-10-23T15:31:11.328Z", "location_count": 1, "location_summary": "Charlottesville, Virginia", "locations": [ { "city": "Charlottesville", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT03882931" }, { "nct_id": "NCT03870672", "title": "rTMS Plus CCFES-mediated Functional Task Practice for Severe Stroke", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke", "Hemiplegia", "Cerebrovascular Accident (CVA)", "Hemiparesis" ], "interventions": [ { "name": "Contralaterally Controlled Functional Electrical Stimulation", "type": "DEVICE" }, { "name": "New rTMS approach", "type": "DEVICE" }, { "name": "Conventional rTMS approach", "type": "DEVICE" }, { "name": "Sham rTMS approach", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 72, "start_date": "2019-05-14", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-08-26", "last_synced_at": "2026-10-23T15:31:11.328Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03870672" }, { "nct_id": "NCT03525613", "title": "A Study to Compare the Efficacy and Safety of Intravitreal APL-2 Therapy With Sham Injections in Patients With Geographic Atrophy (GA) Secondary to Age-Related Macular Degeneration", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Geographic Atrophy" ], "interventions": [ { "name": "APL-2", "type": "DRUG" }, { "name": "Sham Procedure", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Apellis Pharmaceuticals, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "60 Years", "maximum_age": null, "sex": "ALL", "summary": "60 Years and older" }, "enrollment_count": 637, "start_date": "2018-08-31", "completion_date": "2022-06-28", "has_results": true, "last_update_posted_date": "2023-07-06", "last_synced_at": "2026-10-23T15:31:11.328Z", "location_count": 67, "location_summary": "Phoenix, Arizona • Bakersfield, California • Beverly Hills, California + 56 more", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Bakersfield", "state": "California" }, { "city": "Beverly Hills", "state": "California" }, { "city": "Campbell", "state": "California" }, { "city": "Fullerton", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03525613" }, { "nct_id": "NCT06610617", "title": "Neuromodulation of Central Sensory Integration to Improve Postural Control", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Survivorship", "Quality of Life", "Cognitive Deficits, Mild" ], "interventions": [ { "name": "transcranial direct current stimulation (tDCS)", "type": "DEVICE" }, { "name": "Sham tDCS", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": "85 Years", "sex": "FEMALE", "summary": "50 Years to 85 Years · Female only" }, "enrollment_count": 48, "start_date": "2024-10-14", "completion_date": "2025-07-31", "has_results": false, "last_update_posted_date": "2025-11-12", "last_synced_at": "2026-10-23T15:31:11.328Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06610617" }, { "nct_id": "NCT06960317", "title": "Empathy Through Pain Control: Lidocaine Paracervical Block for IUD Placements", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Contraception", "Pain, Acute", "Anesthesia, Local" ], "interventions": [ { "name": "Buffered Lidocaine", "type": "DRUG" }, { "name": "Sham Comparator", "type": "OTHER" }, { "name": "Unbuffered lidocaine", "type": "DRUG" }, { "name": "Xylocaine jelly 2%", "type": "DRUG" }, { "name": "Surgilube", "type": "DRUG" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "University of California, San Diego", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "FEMALE", "summary": "18 Years to 50 Years · Female only" }, "enrollment_count": 204, "start_date": "2025-06-04", "completion_date": "2028-06-30", "has_results": false, "last_update_posted_date": "2025-06-13", "last_synced_at": "2026-10-23T15:31:11.328Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06960317" } ] }