{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sham+Test&page=6", "query": { "intervention": "Sham Test", "page": 6 }, "page_size": 10 }, "pagination": { "page": 6, "page_size": 10, "total_count": 283, "total_pages": 29, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sham+Test&page=7&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Sham+Test&page=5&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-22T02:32:50.187Z", "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": "NCT04606095", "title": "Explosive Synchronization of Brain Network Activity in Chronic Pain", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Fibromyalgia", "Healthy Volunteers" ], "interventions": [ { "name": "EEG", "type": "DIAGNOSTIC_TEST" }, { "name": "Neuroimaging EEG/fMRI (Aim 1)", "type": "DIAGNOSTIC_TEST" }, { "name": "HD-tDCS treatments", "type": "DEVICE" }, { "name": "Sham HD-tDCS treatments", "type": "DEVICE" }, { "name": "Neuroimaging EEG/fMRI (Aim 3)", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "DEVICE" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "19 Years", "maximum_age": "74 Years", "sex": "ALL", "summary": "19 Years to 74 Years" }, "enrollment_count": 150, "start_date": "2020-11-13", "completion_date": "2026-12-20", "has_results": false, "last_update_posted_date": "2026-09-30", "last_synced_at": "2026-10-22T02:32:50.187Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04606095" }, { "nct_id": "NCT04211766", "title": "Fiber and Fish Oil Supplements for the Prevention of Colorectal Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Healthy Subject" ], "interventions": [ { "name": "Dietary Fiber", "type": "DIETARY_SUPPLEMENT" }, { "name": "Fish Oil", "type": "DIETARY_SUPPLEMENT" }, { "name": "Comparator", "type": "OTHER" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "OTHER" ], "sponsor": "Fred Hutchinson Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "50 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "50 Years to 75 Years" }, "enrollment_count": 38, "start_date": "2021-01-05", "completion_date": "2022-08-16", "has_results": true, "last_update_posted_date": "2024-09-27", "last_synced_at": "2026-10-22T02:32:50.187Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT04211766" }, { "nct_id": "NCT05379153", "title": "Testing Laser Therapy for Treatment of Vaginal Dryness in Survivors of Breast Cancer, The Revitalize Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Vaginal Atrophy", "Breast Carcinoma" ], "interventions": [ { "name": "Laser Therapy", "type": "DEVICE" }, { "name": "Sham Intervention", "type": "DEVICE" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Quality of Life Assessment", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Alliance for Clinical Trials in Oncology", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": null, "sex": "FEMALE", "summary": "22 Years and older · Female only" }, "enrollment_count": 250, "start_date": "2026-04-21", "completion_date": "2030-04-30", "has_results": false, "last_update_posted_date": "2026-10-19", "last_synced_at": "2026-10-22T02:32:50.187Z", "location_count": 3, "location_summary": "Des Moines, Iowa • Ann Arbor, Michigan • Columbus, Ohio", "locations": [ { "city": "Des Moines", "state": "Iowa" }, { "city": "Ann Arbor", "state": "Michigan" }, { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT05379153" }, { "nct_id": "NCT06297200", "title": "Low-Intensity Focused Ultrasound and the Complex Patient", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Opioid Use Disorder", "Chronic Pain", "Anxiety Disorder" ], "interventions": [ { "name": "Low-Intensity Focused Ultrasound", "type": "DEVICE" }, { "name": "Low-Intensity Focused Ultrasound - sham", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Virginia Polytechnic Institute and State 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": 25, "start_date": "2024-12-04", "completion_date": "2026-10", "has_results": false, "last_update_posted_date": "2025-11-03", "last_synced_at": "2026-10-22T02:32:50.187Z", "location_count": 1, "location_summary": "Roanoke, Virginia", "locations": [ { "city": "Roanoke", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT06297200" }, { "nct_id": "NCT03049358", "title": "Olfactory Training in Improving Sense of Smell After Radiation Therapy in Patients With Paranasal Sinus or Nasopharyngeal Cancer", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stage 0 Nasopharyngeal Carcinoma", "Stage 0 Paranasal Sinus Cancer", "Stage I Nasopharyngeal Carcinoma", "Stage I Paranasal Sinus Cancer", "Stage II Nasopharyngeal Carcinoma", "Stage II Paranasal Sinus Cancer", "Stage IIA Nasopharyngeal Carcinoma", "Stage IIB Nasopharyngeal Carcinoma", "Stage III Nasopharyngeal Carcinoma", "Stage III Paranasal Sinus Cancer", "Stage IV Nasopharyngeal Carcinoma", "Stage IV Paranasal Sinus Cancer", "Stage IVA Nasopharyngeal Carcinoma", "Stage IVA Paranasal Sinus Cancer", "Stage IVB Nasopharyngeal Carcinoma", "Stage IVB Paranasal Sinus Cancer", "Stage IVC Nasopharyngeal Carcinoma", "Stage IVC Paranasal Sinus Cancer" ], "interventions": [ { "name": "Physiologic Testing", "type": "OTHER" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Sham Intervention", "type": "PROCEDURE" }, { "name": "Therapeutic Procedure", "type": "PROCEDURE" }, { "name": "rose essential oil", "type": "OTHER" }, { "name": "lemon essential oil", "type": "OTHER" }, { "name": "clove essential oil", "type": "OTHER" }, { "name": "eucalyptus essential oil", "type": "OTHER" }, { "name": "canola oil placebo", "type": "OTHER" } ], "intervention_types": [ "OTHER", "PROCEDURE" ], "sponsor": "Stanford University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "19 Years", "maximum_age": null, "sex": "ALL", "summary": "19 Years and older" }, "enrollment_count": 15, "start_date": "2016-12", "completion_date": "2018-10", "has_results": false, "last_update_posted_date": "2019-02-05", "last_synced_at": "2026-10-22T02:32:50.187Z", "location_count": 1, "location_summary": "Palo Alto, California", "locations": [ { "city": "Palo Alto", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03049358" }, { "nct_id": "NCT01694199", "title": "Pulsed Radiofrequency Energy to Treat Post-Bunionectomy Pain", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post-operative Pain" ], "interventions": [ { "name": "Pulsed Radiofrequency Energy (PRFE)", "type": "DEVICE" }, { "name": "No Pulsed Radiofrequency Energy (PRFE)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Regenesis Biomedical, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 139, "start_date": "2012-09", "completion_date": "2012-12", "has_results": true, "last_update_posted_date": "2017-05-02", "last_synced_at": "2026-10-22T02:32:50.187Z", "location_count": 3, "location_summary": "Pasadena, California • Pasadena, Maryland • San Antonio, Texas", "locations": [ { "city": "Pasadena", "state": "California" }, { "city": "Pasadena", "state": "Maryland" }, { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01694199" }, { "nct_id": "NCT05421208", "title": "Cardiovascular Autonomic and Immune Mechanism of Post COVID-19 Tachycardia Syndrome", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post-acute COVID-19 Syndrome", "Postural Tachycardia Syndrome (POTS)", "Long COVID", "SARS CoV 2 Infection" ], "interventions": [ { "name": "Levels of inflammatory cytokine ( IL-6) in post-COVID-19 POTS and controls", "type": "DIAGNOSTIC_TEST" }, { "name": "Levels of inflammatory cytokine ( IL-6) in controls", "type": "DIAGNOSTIC_TEST" }, { "name": "Effect on inflammation after chronic PNS stimulation", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2022-06-01", "completion_date": "2027-06-30", "has_results": false, "last_update_posted_date": "2026-07-15", "last_synced_at": "2026-10-22T02:32:50.187Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT05421208" }, { "nct_id": "NCT06821568", "title": "Home-Based Brain Stimulation for Motoric Cognitive Risk Syndrome", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Alzheimer Disease and Related Dementias", "Cognition", "Mobility Disability" ], "interventions": [ { "name": "Personalized Transcranial Direct Current Stimulation (tDCS)", "type": "OTHER" }, { "name": "Active-Sham", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Hebrew SeniorLife", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "65 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "65 Years to 90 Years" }, "enrollment_count": 128, "start_date": "2025-09-02", "completion_date": "2029-06", "has_results": false, "last_update_posted_date": "2026-07-16", "last_synced_at": "2026-10-22T02:32:50.187Z", "location_count": 1, "location_summary": "Roslindale, Massachusetts", "locations": [ { "city": "Roslindale", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT06821568" }, { "nct_id": "NCT05792020", "title": "Safety, Parameterization, and Mechanism of Transcranial Focused Ultrasound", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Healthy" ], "interventions": [ { "name": "Focused Ultrasound Stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Medical University of South Carolina", "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": 25, "start_date": "2026-07", "completion_date": "2028-12-31", "has_results": false, "last_update_posted_date": "2026-05-22", "last_synced_at": "2026-10-22T02:32:50.187Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05792020" }, { "nct_id": "NCT06286800", "title": "Personalized Transcranial Direct Current Stimulation in Stroke Recovery", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke", "Chronic Stroke", "Hemorrhage Brain", "Ischemic Stroke" ], "interventions": [ { "name": "Transcranial direct current stimulation (tDCS) with OT", "type": "DEVICE" }, { "name": "Sham tDCS with OT", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "The Methodist Hospital Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 80, "start_date": "2024-12-18", "completion_date": "2029-09-30", "has_results": false, "last_update_posted_date": "2026-09-21", "last_synced_at": "2026-10-22T02:32:50.187Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT06286800" } ] }