Retrospective Postoperative ARDS Study at Vanderbilt University

NCT00656071 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 89

Last updated 2012-09-07

No results posted yet for this 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

  • ARDS

Sponsors & Collaborators

  • Vanderbilt University

    lead OTHER

Principal Investigators

  • Christopher G Hughes, M.D. · Vanderbilt University Medical Center

Eligibility

Min Age
11 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-10-31
Primary Completion
2008-08-31
Completion
2008-08-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00656071 on ClinicalTrials.gov