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NCT00351741 · ClinicalTrials.gov registry record · NA
BEST (Burn Center Evaluation of Standard Therapies) Ventilator Mode Study-
A NA study, sponsored by United States Army Institute of Surgical Research.
- Terminated
- Registry status
- NA
- Development phase
- 62
- Enrollment target
NCT00351741: Clinical Trial NA study, sponsored by United States Army Institute of Surgical Research.
NCT00351741 is a NA study that was terminated before completion, run by United States Army Institute of Surgical Research. The registered enrollment target is 62 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00351741, a NA study, was terminated before completion, sponsored by United States Army Institute of Surgical Research.
- TERMINATED
- Registry status
- NA
- Development phase
- 62 participants
- Enrollment target
Study Summary
The purpose of this study is to compare High Frequency Pressure Ventilation (HFPV) to conventional mechanical ventilation. Hypothesis: Patients placed on HFPV will have significantly higher number of ventilator-free days compared to patients placed on a conventional volume mode.
Primary Outcome
The primary end point was ventilator-free days in the first 28 days, defined as the number of days after randomization from day 0 to day 28 alive without ventilator assistance for at least 48 consecutive hrs.
Interventions
- DEVICE Ventilation - High Frequency Percussive Ventilation
- DEVICE Ventilation - ARDSnet
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 62 participants |
| Start Date | 2006-07 |
| Est. Completion | 2010-02 |
| Phase | NA |
Why NCT00351741 stopped before completion
NCT00351741 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 62 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).
The record links to 0 conditions, and to 2 interventions - of which Ventilation - High Frequency Percussive Ventilation is the first listed.
NCT00351741 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00351741 about?
NCT00351741 is a clinical study titled "BEST (Burn Center Evaluation of Standard Therapies) Ventilator Mode Study-". The purpose of this study is to compare High Frequency Pressure Ventilation (HFPV) to conventional mechanical ventilation. Hypothesis: Patients placed on HFPV will have significantly higher number of ventilator-free days compared to patients placed on a conventional volume mode.
What is the current status of trial NCT00351741?
This trial is currently terminated. It is a NA study. The enrollment target is 62 participants. The study started on 2006-07. Estimated completion is 2010-02.
What interventions are being tested in trial NCT00351741?
The interventions under investigation include: Ventilation - High Frequency Percussive Ventilation (DEVICE), Ventilation - ARDSnet (DEVICE).
Who is sponsoring clinical trial NCT00351741?
This trial is sponsored by United States Army Institute of Surgical Research, which has 17 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00351741's enrollment target sits among peer trials
62 1157th of 2000 higher than 837 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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