{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sham+Treatment+Location&page=3", "query": { "intervention": "Sham Treatment Location", "page": 3 }, "page_size": 10 }, "pagination": { "page": 3, "page_size": 10, "total_count": 692, "total_pages": 70, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sham+Treatment+Location&page=4&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sham+Treatment+Location&page=2&page_size=10" }, "source": "remote", "last_synced_at": "2026-11-15T14:51:22.570Z", "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": "NCT04964934", "title": "Phase III Study to Assess AZD9833+ CDK4/6 Inhibitor in HR+/HER2-MBC With Detectable ESR1m Before Progression (SERENA-6)", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "ER-Positive HER2-Negative Breast Cancer" ], "interventions": [ { "name": "AZD9833", "type": "DRUG" }, { "name": "AZD9833 Placebo", "type": "DRUG" }, { "name": "Anastrozole", "type": "DRUG" }, { "name": "Anastrozole placebo", "type": "DRUG" }, { "name": "Letrozole", "type": "DRUG" }, { "name": "Letrozole placebo", "type": "DRUG" }, { "name": "Palbociclib", "type": "DRUG" }, { "name": "Abemaciclib", "type": "DRUG" }, { "name": "Luteinizing hormone-releasing hormone (LHRH) agonist", "type": "DRUG" }, { "name": "Ribociclib", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "AstraZeneca", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "130 Years", "sex": "ALL", "summary": "18 Years to 130 Years" }, "enrollment_count": 315, "start_date": "2021-06-30", "completion_date": "2028-09-01", "has_results": false, "last_update_posted_date": "2026-09-23", "last_synced_at": "2026-11-15T14:51:22.570Z", "location_count": 64, "location_summary": "Phoenix, Arizona • Hot Springs, Arkansas • Little Rock, Arkansas + 56 more", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Hot Springs", "state": "Arkansas" }, { "city": "Little Rock", "state": "Arkansas" }, { "city": "Long Beach", "state": "California" }, { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04964934" }, { "nct_id": "NCT02064452", "title": "Evaluating an Online Parenting Support System Disseminated by Pediatric Practices", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Child Disruptive Behavior Disorders", "Oppositional Defiant Disorder", "Conduct Disorder", "Attention Deficit Hyperactivity Disorder" ], "interventions": [ { "name": "Triple P Online System", "type": "OTHER" }, { "name": "Placebo Comparator", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Oregon Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "3 Years", "maximum_age": null, "sex": "ALL", "summary": "3 Years and older" }, "enrollment_count": 600, "start_date": "2014-05", "completion_date": "2019-03", "has_results": false, "last_update_posted_date": "2019-04-18", "last_synced_at": "2026-11-15T14:51:22.570Z", "location_count": 2, "location_summary": "Eugene, Oregon • Seattle, Washington", "locations": [ { "city": "Eugene", "state": "Oregon" }, { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT02064452" }, { "nct_id": "NCT05004506", "title": "Intra-articular Analgesia Versus Adductor Canal Block for Arthroscopic Knee Surgery", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Post-Operative Pain, Chronic" ], "interventions": [ { "name": "Adductor Canal Block", "type": "DRUG" }, { "name": "Intra-articular Injection", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Loyola University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 100, "start_date": "2016-04-20", "completion_date": "2022-12-31", "has_results": false, "last_update_posted_date": "2022-04-12", "last_synced_at": "2026-11-15T14:51:22.570Z", "location_count": 1, "location_summary": "Maywood, Illinois", "locations": [ { "city": "Maywood", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05004506" }, { "nct_id": "NCT02797678", "title": "Feasibility, Effectiveness and Efficacy of the PowerSleep Device", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleep", "Sleep Disorders Not Due to A Substance or Known Physiological Condition" ], "interventions": [ { "name": "Powersleep", "type": "DEVICE" }, { "name": "Sham Powersleep", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Philips Respironics", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "21 Years to 50 Years" }, "enrollment_count": 62, "start_date": "2016-06", "completion_date": "2017-01", "has_results": true, "last_update_posted_date": "2019-01-11", "last_synced_at": "2026-11-15T14:51:22.570Z", "location_count": 4, "location_summary": "Atlanta, Georgia • Chesterfield, Missouri • St Louis, Missouri + 1 more", "locations": [ { "city": "Atlanta", "state": "Georgia" }, { "city": "Chesterfield", "state": "Missouri" }, { "city": "St Louis", "state": "Missouri" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02797678" }, { "nct_id": "NCT05377411", "title": "SMART Stimulation: Precision Neuromodulation of Cognition in Older Adults", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Aging" ], "interventions": [ { "name": "tDCS", "type": "DEVICE" }, { "name": "cognitive training", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "University of Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "65 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "65 Years to 89 Years" }, "enrollment_count": 33, "start_date": "2023-01-17", "completion_date": "2024-06-03", "has_results": true, "last_update_posted_date": "2025-06-26", "last_synced_at": "2026-11-15T14:51:22.570Z", "location_count": 1, "location_summary": "Gainesville, Florida", "locations": [ { "city": "Gainesville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT05377411" }, { "nct_id": "NCT05503264", "title": "A Study to Evaluate the Efficacy, Safety, Pharmacokinetics (PK), and Pharmacodynamics (PD) of Satralizumab in Participants With Anti-N-methyl-D-aspartic Acid Receptor (NMDAR) or Anti-leucine-rich Glioma-inactivated 1 (LGI1) Encephalitis", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "NMDAR Autoimmune Encephalitis", "LGI1 Autoimmune Encephalitis" ], "interventions": [ { "name": "Satralizumab", "type": "DRUG" }, { "name": "Placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Hoffmann-La Roche", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "12 Years", "maximum_age": null, "sex": "ALL", "summary": "12 Years and older" }, "enrollment_count": 122, "start_date": "2022-09-27", "completion_date": "2028-12-14", "has_results": false, "last_update_posted_date": "2026-10-08", "last_synced_at": "2026-11-15T14:51:22.570Z", "location_count": 11, "location_summary": "Birmingham, Alabama • Newport Beach, California • San Francisco, California + 7 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Newport Beach", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "Aurora", "state": "Colorado" }, { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT05503264" }, { "nct_id": "NCT02589938", "title": "Trial of Acupuncture for Radiation-Induced Xerostomia in Head and Neck Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Radiation-Induced Xerostomia", "Head and Neck Cancer", "Radiation Toxicity", "Oral Complications of Chemotherapy and Head/Neck Radiation" ], "interventions": [ { "name": "Standard Oral Hygiene", "type": "OTHER" }, { "name": "Standard Oral Hygiene + True Acupuncture", "type": "OTHER" }, { "name": "Standard Oral Hygiene + Sham Acupuncture", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 258, "start_date": "2012-11-11", "completion_date": "2022-07-29", "has_results": true, "last_update_posted_date": "2026-02-27", "last_synced_at": "2026-11-15T14:51:22.570Z", "location_count": 36, "location_summary": "Burbank, California • San Francisco, California • San Jose, California + 26 more", "locations": [ { "city": "Burbank", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "San Jose", "state": "California" }, { "city": "San Rafael", "state": "California" }, { "city": "San Rafael", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02589938" }, { "nct_id": "NCT02981017", "title": "Improvement of Outcomes in Draf III/Endoscopic Modified Lothrop Procedure", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Sinusitis", "Frontal Sinusitis" ], "interventions": [ { "name": "Porcine Intestinal submucosal xenograft", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of California, Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2016-11-01", "completion_date": "2019-12-28", "has_results": false, "last_update_posted_date": "2020-10-30", "last_synced_at": "2026-11-15T14:51:22.570Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02981017" }, { "nct_id": "NCT02691143", "title": "The Effect of TheraBand® Kinesiology Tape on Post-manipulation Pain and Range of Motion", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Non-complicated Postural Neck Pain" ], "interventions": [ { "name": "TheraBand Kinesiology Tape", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Sport and Spine Rehab Clinical Research Foundation", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 50, "start_date": "2016-02", "completion_date": "2016-12", "has_results": true, "last_update_posted_date": "2017-03-17", "last_synced_at": "2026-11-15T14:51:22.570Z", "location_count": 1, "location_summary": "Rockville, Maryland", "locations": [ { "city": "Rockville", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT02691143" }, { "nct_id": "NCT03337113", "title": "Working Memory Training Combined With Transcranial Magnetic Stimulation in Smokers", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Tobacco Use Disorder" ], "interventions": [ { "name": "Working Memory Training", "type": "OTHER" }, { "name": "Sham Working Memory Training", "type": "OTHER" }, { "name": "repetitive Transcranial Magnetic Stimulation", "type": "DEVICE" }, { "name": "Sham repetitive Transcranial Magnetic Stimulation", "type": "DEVICE" } ], "intervention_types": [ "OTHER", "DEVICE" ], "sponsor": "Kent State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 50, "start_date": "2018-03-05", "completion_date": "2021-01-31", "has_results": true, "last_update_posted_date": "2022-05-02", "last_synced_at": "2026-11-15T14:51:22.570Z", "location_count": 2, "location_summary": "Providence, Rhode Island", "locations": [ { "city": "Providence", "state": "Rhode Island" }, { "city": "Providence", "state": "Rhode Island" } ], "official_url": "https://clinicaltrials.gov/study/NCT03337113" } ] }