Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Precision Ventilation vs Standard Care for Acute Respiratory Distress Syndrome
NCT06066502 · View on ClinicalTrials.gov ↗
Study Summary
The goal of this interventional study is to compare standard mechanical ventilation to a lung-stress oriented ventilation strategy in patients with Acute Respiratory Distress Syndrome (ARDS). Participants will be ventilated according to one of two different strategies. The main question the study hopes to answer is whether the personalized ventilation strategy helps improve survival.
Conditions Studied
Interventions
- OTHER Precision ventilation
- OTHER Guided usual care ventilation
Study Locations (20)
California
- University of California, San Diego — La Jolla
- University of California, Los Angeles Medical Center — Los Angeles
- Cedar-Sinai Medical Center — Los Angeles
- University of California, San Francisco — San Franciso
Massachusetts
- Tufts Medical Center — Boston
- Massachusetts General Hospital — Boston
- Brigham and Women's Hospital — Boston
- Beth Israel Deaconess Medical Center — Boston
New York
- NYU Lagone Health — New York
- New York City Health + Hospitals/ Bellevue — New York
- Albert Einstein College of Medicine/Montefiore Medical Center — The Bronx
Ohio
- University of Cincinnati — Cincinnati
- Cleveland Clinic Foundation — Cleveland
- Ohio State University Wexner Medical Center — Columbus
North Carolina
- Duke University Medical Center — Durham
- Atrium Health Wake Forest Baptist — Winston-Salem
Arizona
- University of Arizona — Tucson
Illinois
- University of Chicago — Chicago
Michigan
- University of Michigan — Ann Arbor
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 1,100 participants |
| Start Date | 2024-06-24 |
| Est. Completion | 2030-08-31 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06066502
The ClinicalTrials.gov registry entry for NCT06066502 describes a study currently listed as recruiting. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 1,100 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Beth Israel Deaconess Medical Center, which has 434 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Respiratory Failure appearing as the primary indexed condition, and to 2 interventions — of which Precision ventilation is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06066502 reports 20 study locations spanning 9 distinct geographic areas — top geographies include California, Massachusetts, New York. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06066502 about?
NCT06066502 is a clinical study titled "Precision Ventilation vs Standard Care for Acute Respiratory Distress Syndrome". The goal of this interventional study is to compare standard mechanical ventilation to a lung-stress oriented ventilation strategy in patients with Acute Respiratory Distress Syndrome (ARDS). Participants will be ventilated according to one of two different strategies. The main question the study ho...
What is the current status of trial NCT06066502?
This trial is currently recruiting. It is a Phase 3 study. The enrollment target is 1,100 participants. The study started on 2024-06-24. Estimated completion is 2030-08-31.
What conditions does trial NCT06066502 study?
This clinical trial studies the following conditions: Respiratory Failure, Acute Respiratory Distress Syndrome. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06066502?
The interventions under investigation include: Precision ventilation (OTHER), Guided usual care ventilation (OTHER). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06066502?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 434 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06066502 being conducted?
This trial has 20 study locations across Arizona, California, Illinois, Massachusetts, Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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