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NCT00656071 · ClinicalTrials.gov registry record

Retrospective Postoperative ARDS Study at Vanderbilt University

A clinical trial of ARDS, sponsored by Vanderbilt University.

Completed
Registry status
89
Enrollment target
1
Study location

NCT00656071 is a study of ARDS that has completed, run by Vanderbilt University. The registered enrollment target is 89 participants, below the 581-participant average among 14 other ARDS trials with a reported enrollment target (85% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT00656071, a study of ARDS, has completed, sponsored by Vanderbilt University.

COMPLETED
Registry status
89 participants
Enrollment target
1
Study location

Study Summary

By examining the intraoperative anesthetic characteristics of patients who developed ARDS postoperatively, we hope to identify variables which have a positive or negative association on the development of ARDS.

Conditions Studied

Study Locations (1)

Tennessee

  • Vanderbilt University Medical Center - Nashville

Trial Details

FieldValue
Enrollment Target 89 participants
Start Date 2007-10
Est. Completion 2008-08

Sponsor

Vanderbilt University

430 total trials

What the Registry Record Tells You About NCT00656071

The ClinicalTrials.gov registry entry for NCT00656071 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 89 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 581-participant average among 14 other ARDS trials with a reported enrollment target (85% lower). The listed sponsor is Vanderbilt University, which has 430 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with ARDS appearing as the primary indexed condition, and to 0 interventions.

NCT00656071 reports 1 study location spanning 1 distinct geographic area - top geographies include Tennessee.

Frequently Asked Questions

What is clinical trial NCT00656071 about?

NCT00656071 is a clinical study titled "Retrospective Postoperative ARDS Study at Vanderbilt University". By examining the intraoperative anesthetic characteristics of patients who developed ARDS postoperatively, we hope to identify variables which have a positive or negative association on the development of ARDS.

What is the current status of trial NCT00656071?

This trial is currently completed. The enrollment target is 89 participants. The study started on 2007-10. Estimated completion is 2008-08.

What conditions does trial NCT00656071 study?

This clinical trial studies the following conditions: ARDS.

Who is sponsoring clinical trial NCT00656071?

This trial is sponsored by Vanderbilt University, which has 430 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00656071 being conducted?

This trial has 1 study location across Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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