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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 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.

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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.

Interventions

  • DEVICE Ventilation - High Frequency Percussive Ventilation
  • DEVICE Ventilation - ARDSnet

Trial Details

FieldValue
Enrollment Target 62 participants
Start Date 2006-07
Est. Completion 2010-02
Phase NA

What the Registry Record Tells You About NCT00351741

The ClinicalTrials.gov registry entry for NCT00351741 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 62 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is United States Army Institute of Surgical Research, which has 17 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Ventilation - High Frequency Percussive Ventilation is the first listed.

NCT00351741 reports 0 study locations.

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.