{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Head+of+Bed+Up", "query": { "intervention": "Head of Bed Up" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 17, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Head+of+Bed+Up&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-23T12:42:48.633Z", "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": "NCT02591641", "title": "Use of a Shear Reduction Surface in Pre-hospital Transport", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Shear Strength" ], "interventions": [ { "name": "Anti-shear mattress overlay", "type": "DEVICE" }, { "name": "Standard of Care", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 30, "start_date": "2015-11", "completion_date": "2016-11", "has_results": false, "last_update_posted_date": "2017-03-03", "last_synced_at": "2026-09-23T12:42:48.633Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT02591641" }, { "nct_id": "NCT05321719", "title": "Multi-Media Parent-based Intervention to Promote Dental Hygiene Among Young Children: BeReady2Smile II", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Plaque" ], "interventions": [ { "name": "Comparison Condition", "type": "BEHAVIORAL" }, { "name": "BeReady2Smile video only", "type": "BEHAVIORAL" }, { "name": "BeReady2Smile video and BeReady2Smile app completely self-guided", "type": "BEHAVIORAL" }, { "name": "\"Complete\" BeReady2Smile video and BeReady2Smile app guided by a Coach", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Oregon Research Behavioral Intervention Strategies, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 228, "start_date": "2023-04-10", "completion_date": "2024-04-30", "has_results": false, "last_update_posted_date": "2025-10-08", "last_synced_at": "2026-09-23T12:42:48.633Z", "location_count": 1, "location_summary": "Springfield, Oregon", "locations": [ { "city": "Springfield", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT05321719" }, { "nct_id": "NCT05408871", "title": "Non-invasive Measurement of PD-L1 Levels With Positron Emission Tomography (PET) in Head and Neck Malignancies and Intracranial Metastases", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Cancer Head Neck", "Metastatic Cancer", "Metastatic Lung Cancer" ], "interventions": [ { "name": "adnectin 18F-BMS-986192 Head and Neck Cancer", "type": "DRUG" }, { "name": "adnectin 18F-BMS-986192 Brain Metastases", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 7, "start_date": "2023-02-21", "completion_date": "2024-01-31", "has_results": false, "last_update_posted_date": "2024-02-15", "last_synced_at": "2026-09-23T12:42:48.633Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT05408871" }, { "nct_id": "NCT04340258", "title": "Trial Combining Pembrolizumab and Cesium 131 Brachytherapy With Salvage Surgery in HNSCC", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "HNSCC" ], "interventions": [ { "name": "Cesium-131", "type": "DEVICE" }, { "name": "Pembrolizumab", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "DRUG" ], "sponsor": "University of Cincinnati", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "19 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "19 Years to 90 Years" }, "enrollment_count": 50, "start_date": "2021-02-04", "completion_date": "2026-09-04", "has_results": false, "last_update_posted_date": "2026-06-09", "last_synced_at": "2026-09-23T12:42:48.633Z", "location_count": 2, "location_summary": "Cincinnati, Ohio • Philadelphia, Pennsylvania", "locations": [ { "city": "Cincinnati", "state": "Ohio" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04340258" }, { "nct_id": "NCT05070143", "title": "Mini-treatment Experiments to Clarify How to Assist People to Habit Formation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleep Disorder", "Circadian Dysregulation", "Habit, Good Sleep" ], "interventions": [ { "name": "RISE-UP Routine", "type": "BEHAVIORAL" }, { "name": "Awareness Training", "type": "BEHAVIORAL" }, { "name": "Vigilant Monitoring", "type": "BEHAVIORAL" }, { "name": "Implementation Intentions", "type": "BEHAVIORAL" }, { "name": "Values-based Approach", "type": "BEHAVIORAL" }, { "name": "Brief Education", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of California, Berkeley", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 286, "start_date": "2021-10-07", "completion_date": "2023-05-01", "has_results": false, "last_update_posted_date": "2023-05-10", "last_synced_at": "2026-09-23T12:42:48.633Z", "location_count": 1, "location_summary": "Berkeley, California", "locations": [ { "city": "Berkeley", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT05070143" }, { "nct_id": "NCT00223717", "title": "Treatment of Supine Hypertension in Autonomic Failure", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Hypertension" ], "interventions": [ { "name": "Clonidine", "type": "DRUG" }, { "name": "Nitroglycerin transdermal", "type": "DRUG" }, { "name": "Dipyridamole/ Aspirin (Aggrenox)", "type": "DRUG" }, { "name": "Desmopressin (DDAVP)", "type": "DRUG" }, { "name": "Sildenafil", "type": "DRUG" }, { "name": "Nifedipine", "type": "DRUG" }, { "name": "Hydralazine", "type": "DRUG" }, { "name": "Hydrochlorothiazide", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Bosentan", "type": "DRUG" }, { "name": "Diltiazem", "type": "DRUG" }, { "name": "Eplerenone", "type": "DRUG" }, { "name": "guanfacine", "type": "DRUG" }, { "name": "L-arginine", "type": "DIETARY_SUPPLEMENT" }, { "name": "captopril", "type": "DRUG" }, { "name": "carbidopa", "type": "DRUG" }, { "name": "losartan", "type": "DRUG" }, { "name": "metoprolol tartrate", "type": "DRUG" }, { "name": "nebivolol hydrochloride", "type": "DRUG" }, { "name": "prazosin hydrochloride", "type": "DRUG" }, { "name": "tamsulosin hydrochloride", "type": "DRUG" }, { "name": "Head-up tilt.", "type": "OTHER" }, { "name": "aliskiren", "type": "DRUG" }, { "name": "Local heat stress", "type": "OTHER" } ], "intervention_types": [ "DRUG", "DIETARY_SUPPLEMENT", "OTHER" ], "sponsor": "Vanderbilt University", "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": 152, "start_date": "2001-01", "completion_date": "2017-01", "has_results": false, "last_update_posted_date": "2017-10-13", "last_synced_at": "2026-09-23T12:42:48.633Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT00223717" }, { "nct_id": "NCT05731986", "title": "Spinal Cord Transcutaneous Stimulation Effect on Blood Pressure in Acute Spinal Cord Injury (SCI)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injuries", "Spinal Cord Diseases", "Trauma, Nervous System", "Nervous System Diseases", "Central Nervous System Diseases", "Hypotension", "Orthostatic Hypotension", "Cardiovascular Diseases", "Acute Spinal Cord Injury", "Blood Pressure" ], "interventions": [ { "name": "Orthostatic challenge", "type": "DIAGNOSTIC_TEST" }, { "name": "Biostim-5 transcutaneous spinal stimulation - Mapping", "type": "DEVICE" }, { "name": "Biostim-5 transcutaneous spinal stimulation - \"Optimal\" testing", "type": "DEVICE" }, { "name": "Biostim-5 transcutaneous spinal stimulation - \"Sham\" testing", "type": "DEVICE" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "DEVICE" ], "sponsor": "Kessler Foundation", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 12, "start_date": "2023-12-01", "completion_date": "2026-08", "has_results": false, "last_update_posted_date": "2025-09-02", "last_synced_at": "2026-09-23T12:42:48.633Z", "location_count": 1, "location_summary": "West Orange, New Jersey", "locations": [ { "city": "West Orange", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT05731986" }, { "nct_id": "NCT01593657", "title": "Mindful Movement and Breathing to Improve Outcomes of Gynecologic Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Gynecologic Malignancy", "Abdominal Surgery by Laparotomy", "Pain", "Psychological Distress", "Lung Function", "Surgical Complications" ], "interventions": [ { "name": "Mindful Movement and Breathing program", "type": "OTHER" }, { "name": "Questionnaire administration", "type": "OTHER" }, { "name": "The Observer Mobility Scale", "type": "PROCEDURE" }, { "name": "Volumetric Incentive Spirometry", "type": "PROCEDURE" } ], "intervention_types": [ "OTHER", "PROCEDURE" ], "sponsor": "Wake Forest University Health Sciences", "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": 10, "start_date": "2012-05", "completion_date": "2013-03", "has_results": false, "last_update_posted_date": "2018-07-03", "last_synced_at": "2026-09-23T12:42:48.633Z", "location_count": 1, "location_summary": "Winston-Salem, North Carolina", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT01593657" }, { "nct_id": "NCT05489575", "title": "CPAP for the Treatment of Supine Hypertension", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Autonomic Failure", "Pure Autonomic Failure", "Multiple System Atrophy", "Parkinson Disease", "Supine Hypertension", "Neurogenic Orthostatic Hypotension" ], "interventions": [ { "name": "Active CPAP", "type": "DEVICE" }, { "name": "Sham CPAP", "type": "DEVICE" }, { "name": "Sleeping in a head-up tilt (HUT) position", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "40 Years to 80 Years" }, "enrollment_count": 59, "start_date": "2022-06-23", "completion_date": "2027-08-31", "has_results": false, "last_update_posted_date": "2026-04-07", "last_synced_at": "2026-09-23T12:42:48.633Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT05489575" }, { "nct_id": "NCT05284084", "title": "Prevention of Broncho-aspiration (BA) in Adult Subjects During Their ICU Stay", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Bronchial Aspiration" ], "interventions": [ { "name": "Bed Head elevation, H2 blockers and mouth wash", "type": "OTHER" }, { "name": "Data collection for comparison", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Marshall University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 159, "start_date": "2021-08-03", "completion_date": "2021-11-02", "has_results": false, "last_update_posted_date": "2023-04-04", "last_synced_at": "2026-09-23T12:42:48.633Z", "location_count": 1, "location_summary": "Huntington, West Virginia", "locations": [ { "city": "Huntington", "state": "West Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT05284084" } ] }