{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=EQ-5D", "query": { "intervention": "EQ-5D" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 20, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=EQ-5D&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-06T02:24:45.452Z", "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": "NCT03552484", "title": "In-Home Care for Patients With PSP and Related Disorders", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Progressive Supranuclear Palsy", "Dementia With Lewy Bodies", "Multiple System Atrophy", "Corticobasal Syndrome", "Atypical Parkinson Disease" ], "interventions": [ { "name": "Home Visit Program", "type": "BEHAVIORAL" }, { "name": "Usual Care/Online Survey", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Rush University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 56, "start_date": "2018-05-30", "completion_date": "2020-12-31", "has_results": true, "last_update_posted_date": "2024-04-01", "last_synced_at": "2026-09-06T02:24:45.452Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03552484" }, { "nct_id": "NCT05617716", "title": "Spine Radiosurgery for Symptomatic Metastatic Neoplasms", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Metastatic Neoplasm to the Spine", "Metastatic Neoplasm" ], "interventions": [ { "name": "Conventional external beam radiation therapy dose (EBRT)", "type": "RADIATION" }, { "name": "Spine radiosurgery/stereotactic body radiation therapy standard dose", "type": "RADIATION" }, { "name": "Spine radiosurgery/stereotactic body radiation therapy high dose", "type": "RADIATION" } ], "intervention_types": [ "RADIATION" ], "sponsor": "University of Oklahoma", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 240, "start_date": "2025-09-09", "completion_date": "2029-09-30", "has_results": false, "last_update_posted_date": "2025-10-20", "last_synced_at": "2026-09-06T02:24:45.452Z", "location_count": 2, "location_summary": "Baltimore, Maryland • Oklahoma City, Oklahoma", "locations": [ { "city": "Baltimore", "state": "Maryland" }, { "city": "Oklahoma City", "state": "Oklahoma" } ], "official_url": "https://clinicaltrials.gov/study/NCT05617716" }, { "nct_id": "NCT04046575", "title": "Radiation Dose Intensification With Accelerated Hypofractionated Intensity Modulated Radiation Therapy and Concurrent Carboplatin and Paclitaxel for Inoperable Esophageal Cancer", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Esophagus Cancer", "Esophageal Cancer", "Cancer of the Esophagus" ], "interventions": [ { "name": "Intensity Modulated Radiation Therapy", "type": "RADIATION" }, { "name": "Carboplatin", "type": "DRUG" }, { "name": "MD Anderson Symptom Inventory (MDASI)-Plus module", "type": "OTHER" }, { "name": "EuroQol (EQ-5D)", "type": "OTHER" }, { "name": "SF-12", "type": "OTHER" }, { "name": "MOS Social Support Measure", "type": "OTHER" }, { "name": "CES-D", "type": "OTHER" }, { "name": "Blood for ctDNA (optional)", "type": "PROCEDURE" }, { "name": "Blood for SCCA", "type": "PROCEDURE" }, { "name": "Paclitaxel", "type": "DRUG" } ], "intervention_types": [ "RADIATION", "DRUG", "OTHER", "PROCEDURE" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 12, "start_date": "2019-11-07", "completion_date": "2029-11-20", "has_results": false, "last_update_posted_date": "2026-07-13", "last_synced_at": "2026-09-06T02:24:45.452Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT04046575" }, { "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": "2026-09-06T02:24:45.452Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT05421208" }, { "nct_id": "NCT00115505", "title": "Quality of Life, Employment, and Informal Care Costs in Women Who Are Receiving Chemotherapy for Breast Cancer", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Breast Carcinoma" ], "interventions": [ { "name": "quality-of-life assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Alliance for Clinical Trials in Oncology", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 307, "start_date": "2005-10", "completion_date": "2016-06", "has_results": false, "last_update_posted_date": "2017-08-18", "last_synced_at": "2026-09-06T02:24:45.452Z", "location_count": 227, "location_summary": "Mobile, Alabama • Fort Smith, Arkansas • Fresno, California + 154 more", "locations": [ { "city": "Mobile", "state": "Alabama" }, { "city": "Fort Smith", "state": "Arkansas" }, { "city": "Fresno", "state": "California" }, { "city": "Modesto", "state": "California" }, { "city": "Redding", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00115505" }, { "nct_id": "NCT02962154", "title": "Neurocardiac Interactions Evaluated by Anatomic and Physiologic MRI Assessment", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Ischemia", "Stress, Mental" ], "interventions": [ { "name": "Coronary CT Angiography", "type": "RADIATION" }, { "name": "Mood Symptom Scale", "type": "OTHER" }, { "name": "Anxiety Symptom Scale", "type": "OTHER" }, { "name": "Chronic Stress Inventories", "type": "OTHER" }, { "name": "Psychosocial Function Questionnaires", "type": "OTHER" }, { "name": "General Health and quality of life questionnaires", "type": "OTHER" }, { "name": "Magnetic Resonance Imaging", "type": "OTHER" } ], "intervention_types": [ "RADIATION", "OTHER" ], "sponsor": "Weill Medical College of Cornell University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": null, "sex": "ALL", "summary": "50 Years and older" }, "enrollment_count": 0, "start_date": "2016-02", "completion_date": "2018-01", "has_results": false, "last_update_posted_date": "2018-01-09", "last_synced_at": "2026-09-06T02:24:45.452Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02962154" }, { "nct_id": "NCT03801356", "title": "Threshold Response of Lumbar Selective Nerve Root Block in Predicting Good Outcome Following Lumbar Foraminotomy", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Back Pain", "Radiculopathy Lumbar", "Degenerative Lumbar Spinal Stenosis" ], "interventions": [ { "name": "Selective Nerve Root Block", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "The Cleveland Clinic", "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": 11, "start_date": "2018-08-23", "completion_date": "2020-12-15", "has_results": true, "last_update_posted_date": "2023-07-21", "last_synced_at": "2026-09-06T02:24:45.452Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT03801356" }, { "nct_id": "NCT06401239", "title": "Investigating Dyadic Expectations About ARF Survivorship (IDEAS)", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Acute Respiratory Failure", "Caregiving Stress", "Mental Health Issue" ], "interventions": [ { "name": "Dyadic expectations about the ARF survivor's perceived health 6 months after hospital discharge", "type": "OTHER" }, { "name": "Self-efficacy", "type": "OTHER" }, { "name": "Concordant expectations/shared appraisal of ARF survivor's health 6 months after hospital discharge", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 235, "start_date": "2024-07-23", "completion_date": "2027-07", "has_results": false, "last_update_posted_date": "2026-02-05", "last_synced_at": "2026-09-06T02:24:45.452Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT06401239" }, { "nct_id": "NCT02562027", "title": "SBRT (Stereotactic Body Radiation Therapy) vs. Surgery in High Risk Patients With Early Stage Lung Cancer", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Carcinoma, Non-Small-Cell-Lung", "Non-Small Cell Lung Cancer", "Nonsmall Cell Lung Cancer" ], "interventions": [ { "name": "European Organization for Research and Treatment of Cancer Quality of Life Questionnaire C30", "type": "BEHAVIORAL" }, { "name": "European Organization for Research and Treatment of Cancer Quality of Life Questionnaire LC-13", "type": "BEHAVIORAL" }, { "name": "Modified Medical Research Council", "type": "BEHAVIORAL" }, { "name": "EQ-5D", "type": "BEHAVIORAL" }, { "name": "Center for Epidemiological Studies Depression Scale", "type": "BEHAVIORAL" }, { "name": "Medical Outcomes Study Social Support Survey", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Washington University School of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 217, "start_date": "2015-09-11", "completion_date": "2020-11-01", "has_results": false, "last_update_posted_date": "2021-04-08", "last_synced_at": "2026-09-06T02:24:45.452Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT02562027" }, { "nct_id": "NCT01417507", "title": "Natural History of Brain Function, Quality of Life, and Seizure Control in Patients With Brain Tumor Who Have Undergone Surgery", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Adult Diffuse Astrocytoma", "Adult Mixed Glioma", "Adult Oligodendroglioma", "Cognitive/Functional Effects", "Neurotoxicity", "Psychosocial Effects of Cancer and Its Treatment", "Seizure" ], "interventions": [ { "name": "cognitive assessment", "type": "PROCEDURE" }, { "name": "magnetic resonance imaging", "type": "PROCEDURE" }, { "name": "laboratory biomarker analysis", "type": "OTHER" }, { "name": "questionnaire administration", "type": "OTHER" }, { "name": "quality-of-life assessment", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "Radiation Therapy Oncology Group", "sponsor_class": "NETWORK", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 82, "start_date": "2011-10", "completion_date": "2014-12", "has_results": false, "last_update_posted_date": "2015-03-18", "last_synced_at": "2026-09-06T02:24:45.452Z", "location_count": 39, "location_summary": "Birmingham, Alabama • Mobile, Alabama • Phoenix, Arizona + 29 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Birmingham", "state": "Alabama" }, { "city": "Mobile", "state": "Alabama" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Phoenix", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT01417507" } ] }