{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Volume+Controlled+Mode&page=2", "query": { "intervention": "Volume Controlled Mode", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Volume+Controlled+Mode&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-07T07:14:54.778Z", "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": "NCT07656259", "title": "COMPARE-VENT Feasibility Pilot Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Respiration Failure", "Cardio Vascular Disease", "Cardiogenic Pulmonary Oedema", "Critical Illness", "Mechanical Ventilation", "Cardiogenic Shock", "Cardiopulmonary" ], "interventions": [ { "name": "Volume Controlled Mode", "type": "OTHER" }, { "name": "Pressure Controlled Mode", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 75, "start_date": "2026-07-01", "completion_date": "2027-06-30", "has_results": false, "last_update_posted_date": "2026-08-10", "last_synced_at": "2026-09-07T07:14:54.778Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT07656259" }, { "nct_id": "NCT02158923", "title": "Individualized Perioperative Open Lung Ventilatory Strategy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Moderated-high Risk of Postoperative Pulmonary Complication", "Abdominal Surgery Expected More Than Two Hours" ], "interventions": [ { "name": "Alveolar recruitment maneuver", "type": "PROCEDURE" }, { "name": "Calculation of optimal PEEP", "type": "PROCEDURE" }, { "name": "Postoperative CPAP", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Fundación para la Investigación del Hospital Clínico de Valencia", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 920, "start_date": "2014-09", "completion_date": "2016-04", "has_results": false, "last_update_posted_date": "2016-05-17", "last_synced_at": "2026-09-07T07:14:54.778Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT02158923" }, { "nct_id": "NCT05890677", "title": "The LYMPH Trial - Microsurgical Versus Conservative Treatment of Chronic Breast Cancer Associated Lymphedema", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lymphedema, Breast Cancer" ], "interventions": [ { "name": "Surgical Intervention", "type": "PROCEDURE" }, { "name": "Conservative Complex Physical Decongestion Therapy", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University Hospital, Basel, Switzerland", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 280, "start_date": "2023-07-14", "completion_date": "2036-06", "has_results": false, "last_update_posted_date": "2026-06-04", "last_synced_at": "2026-09-07T07:14:54.778Z", "location_count": 4, "location_summary": "New Haven, Connecticut • Boston, Massachusetts • St Louis, Missouri + 1 more", "locations": [ { "city": "New Haven", "state": "Connecticut" }, { "city": "Boston", "state": "Massachusetts" }, { "city": "St Louis", "state": "Missouri" }, { "city": "Rochester", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05890677" }, { "nct_id": "NCT00351741", "title": "BEST (Burn Center Evaluation of Standard Therapies) Ventilator Mode Study-", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Burns" ], "interventions": [ { "name": "Ventilation - High Frequency Percussive Ventilation", "type": "DEVICE" }, { "name": "Ventilation - ARDSnet", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "United States Army Institute of Surgical Research", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 62, "start_date": "2006-07", "completion_date": "2010-02", "has_results": true, "last_update_posted_date": "2015-09-21", "last_synced_at": "2026-09-07T07:14:54.778Z", "location_count": 1, "location_summary": "Fort Sam Houston, Texas", "locations": [ { "city": "Fort Sam Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00351741" }, { "nct_id": "NCT03600194", "title": "Pilot Study Comparing the Effectiveness of Two Different Methods of Acoustic Stimulation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sleep Deprivation", "Insufficient Sleep Syndrome", "Healthy" ], "interventions": [ { "name": "PowerSleep Stim", "type": "DEVICE" }, { "name": "Northwestern Stim", "type": "DEVICE" }, { "name": "PowerSleep Sham", "type": "DEVICE" }, { "name": "NorthWestern Sham", "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": 38, "start_date": "2018-06-01", "completion_date": "2019-07-25", "has_results": true, "last_update_posted_date": "2021-06-14", "last_synced_at": "2026-09-07T07:14:54.778Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03600194" }, { "nct_id": "NCT00793013", "title": "Airway Pressure Release Ventilation (APRV) Compared to ARDSnet Ventilation", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Acute Lung Injury", "Adult Respiratory Distress Syndrome", "Kidney Injury" ], "interventions": [ { "name": "Volume-Cycled Assist-Control (AC) mode", "type": "DEVICE" }, { "name": "Airway Pressure Release Ventilation (APRV) mode", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Tennessee, Chattanooga", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 0, "start_date": "2020-11-02", "completion_date": "2020-11-02", "has_results": false, "last_update_posted_date": "2020-11-04", "last_synced_at": "2026-09-07T07:14:54.778Z", "location_count": 1, "location_summary": "Chattanooga, Tennessee", "locations": [ { "city": "Chattanooga", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT00793013" }, { "nct_id": "NCT00407030", "title": "IncobotulinumtoxinA (Xeomin) Versus Placebo in the Treatment of Cervical Dystonia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Cervical Dystonia" ], "interventions": [ { "name": "incobotulinumtoxinA (Xeomin) (240 Units)", "type": "DRUG" }, { "name": "incobotulinumtoxinA (Xeomin) (120 Units)", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Merz Pharmaceuticals GmbH", "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": 233, "start_date": "2006-07", "completion_date": "2009-06", "has_results": true, "last_update_posted_date": "2013-07-19", "last_synced_at": "2026-09-07T07:14:54.778Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00407030" }, { "nct_id": "NCT05563779", "title": "Mode Of Ventilation During Critical IllnEss Pilot Trial", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Respiratory Failure" ], "interventions": [ { "name": "Volume Control mode", "type": "OTHER" }, { "name": "Pressure Control mode", "type": "OTHER" }, { "name": "Adaptive Pressure Control mode", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 566, "start_date": "2022-11-01", "completion_date": "2023-08-28", "has_results": true, "last_update_posted_date": "2026-02-23", "last_synced_at": "2026-09-07T07:14:54.778Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT05563779" }, { "nct_id": "NCT05639556", "title": "Strength and Muscle Related Outcomes for Nutrition and Lung Function in CF", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cystic Fibrosis" ], "interventions": [ { "name": "BMI and lean mass index from DXA", "type": "DIAGNOSTIC_TEST" }, { "name": "Anthropometric Measurements", "type": "DIAGNOSTIC_TEST" }, { "name": "Hand-grip strength", "type": "DIAGNOSTIC_TEST" }, { "name": "Six-minute walk Test", "type": "DIAGNOSTIC_TEST" }, { "name": "Sit-to-Stand Test", "type": "DIAGNOSTIC_TEST" }, { "name": "Short physical performance battery (SPPB)", "type": "DIAGNOSTIC_TEST" }, { "name": "BIA Sub-study", "type": "DIAGNOSTIC_TEST" }, { "name": "Accelerometry to assess physical activity", "type": "DIAGNOSTIC_TEST" }, { "name": "Gastrointestinal (GI) and nutrition questionnaires:", "type": "OTHER" }, { "name": "Psychosocial questionnaire: PHQ-8", "type": "OTHER" }, { "name": "Psychosocial questionnaire: GAD-7", "type": "OTHER" }, { "name": "Psychosocial questionnaire: The Treatment Self-Regulation Questionnaire (TSRQ)", "type": "OTHER" }, { "name": "Psychosocial questionnaire: CF Fatalism Scale", "type": "OTHER" }, { "name": "Psychosocial questionnaire: Body Esteem Scale for Adolescents and Adults (BESAA)", "type": "OTHER" }, { "name": "12-month Questionnaire", "type": "OTHER" }, { "name": "Oral glucose tolerance testing (OGTT)", "type": "OTHER" }, { "name": "Continuous glucose monitoring (CGM)", "type": "DEVICE" }, { "name": "Chest CT scans (When available within the past 6 months in medical records)", "type": "DIAGNOSTIC_TEST" }, { "name": "Hologic Dual X-Ray Absorptiometry (DXA)", "type": "DIAGNOSTIC_TEST" }, { "name": "Ultrasound Sub-study of assessment of appendage muscles using ultrasound", "type": "DIAGNOSTIC_TEST" }, { "name": "Psychosocial questionnaire: Hunger Vital Sign questionnaire", "type": "DIAGNOSTIC_TEST" }, { "name": "Respiratory symptom questionnaire: CRISS", "type": "OTHER" }, { "name": "Spirometry", "type": "DIAGNOSTIC_TEST" }, { "name": "Psychosocial questionnaire: Additional Health Questionnaire", "type": "OTHER" }, { "name": "CF Management Questionnaire", "type": "OTHER" }, { "name": "Food Frequency Questionnaire", "type": "OTHER" } ], "intervention_types": [ "DIAGNOSTIC_TEST", "OTHER", "DEVICE" ], "sponsor": "Jaeb Center for Health Research", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 300, "start_date": "2023-04-20", "completion_date": "2028-12", "has_results": false, "last_update_posted_date": "2026-03-13", "last_synced_at": "2026-09-07T07:14:54.778Z", "location_count": 23, "location_summary": "Tucson, Arizona • Little Rock, Arkansas • Atlanta, Georgia + 19 more", "locations": [ { "city": "Tucson", "state": "Arizona" }, { "city": "Little Rock", "state": "Arkansas" }, { "city": "Atlanta", "state": "Georgia" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Iowa City", "state": "Iowa" } ], "official_url": "https://clinicaltrials.gov/study/NCT05639556" }, { "nct_id": "NCT06063122", "title": "Development of a Therapeutic Device to Improve Speech Sound Differentiation in Preterm Infants", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Premature Birth" ], "interventions": [ { "name": "smallTalk NICU Active", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Thrive Neuromedical, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "32 Weeks", "maximum_age": "35 Weeks", "sex": "ALL", "summary": "32 Weeks to 35 Weeks" }, "enrollment_count": 203, "start_date": "2024-03-08", "completion_date": "2026-02-01", "has_results": false, "last_update_posted_date": "2025-09-10", "last_synced_at": "2026-09-07T07:14:54.778Z", "location_count": 2, "location_summary": "Atlanta, Georgia • Chagrin Falls, Ohio", "locations": [ { "city": "Atlanta", "state": "Georgia" }, { "city": "Chagrin Falls", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT06063122" } ] }