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NCT00127491 · ClinicalTrials.gov registry record · NA
Mechanical Ventilation, Directed by Esophageal Pressure Measurements, in Patients With Acute Lung Injury
A NA study of Acute Respiratory Distress Syndrome and Acute Lung Injury, sponsored by Beth Israel Deaconess Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 63
- Enrollment target
- 1
- Study location
NCT00127491: Completed NA study of Acute Respiratory Distress Syndrome and Acute Lung Injury, sponsored by Beth Israel Deaconess Medical Center.
NCT00127491 is a NA study of Acute Respiratory Distress Syndrome and Acute Lung Injury that has completed, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 63 participants, below the 365-participant average among 31 other Acute Respiratory Distress Syndrome trials with a reported enrollment target (83% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00127491, a NA study of Acute Respiratory Distress Syndrome and Acute Lung Injury, has completed, sponsored by Beth Israel Deaconess Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 63 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to see whether esophageal pressure (PES) measurements will allow the investigators to choose the best method of mechanical ventilation in patients with acute lung injury (ALI).
Conditions Studied
Interventions
- PROCEDURE Placement of an esophageal balloon measurements
- OTHER Low tidal volume ventilation
- OTHER Transpulmonary pressure-directed ventilation (EPVent)
Study Locations (1)
Massachusetts
- Beth Israel Deaconess Medical Center - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 63 participants |
| Start Date | 2004-05 |
| Est. Completion | 2010-05 |
| Phase | NA |
What the finished NCT00127491 record still lists
NCT00127491 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 63 participants, a relatively small participant target, below the 365-participant average among 31 other Acute Respiratory Distress Syndrome trials with a reported enrollment target (83% lower).
The record links to 2 conditions, with Acute Respiratory Distress Syndrome appearing as the primary indexed condition, and to 3 interventions - of which Placement of an esophageal balloon measurements is the first listed.
NCT00127491 reports a single indexed study location in Massachusetts.
Frequently Asked Questions
What is clinical trial NCT00127491 about?
NCT00127491 is a clinical study titled "Mechanical Ventilation, Directed by Esophageal Pressure Measurements, in Patients With Acute Lung Injury". The purpose of this study is to see whether esophageal pressure (PES) measurements will allow the investigators to choose the best method of mechanical ventilation in patients with acute lung injury (ALI).
What is the current status of trial NCT00127491?
This trial is currently completed. It is a NA study. The enrollment target is 63 participants. The study started on 2004-05. Estimated completion is 2010-05.
What conditions does trial NCT00127491 study?
This clinical trial studies the following conditions: Acute Respiratory Distress Syndrome, Acute Lung Injury.
What interventions are being tested in trial NCT00127491?
The interventions under investigation include: Placement of an esophageal balloon measurements (PROCEDURE), Low tidal volume ventilation (OTHER), Transpulmonary pressure-directed ventilation (EPVent) (OTHER).
Who is sponsoring clinical trial NCT00127491?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT00127491 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Where NCT00127491's enrollment target sits among peer trials
63 18th of 31 higher than 14 of 31 other Acute Respiratory Distress Syndrome trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Acute Respiratory Distress Syndrome 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.
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