ClinicalTrials.Veeva

Menu

Retrospective Postoperative ARDS Study at Vanderbilt University

Vanderbilt University logo

Vanderbilt University

Status

Completed

Conditions

ARDS

Study type

Observational

Funder types

Other

Identifiers

NCT00656071
CHughes-PGY2

Details and patient eligibility

About

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.

Full description

Acute respiratory distress syndrome (ARDS) is a pulmonary disease process that affects post-surgical patients in the intensive care unit and leads to significant patient morbidity and mortality and hospital cost. Extensive research has been conducted in the diagnosis and treatment of ARDS. To date, however, very little research examining the effect of the operative course on the development of ARDS has been reported. 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. Once identified, the variables can be confirmed by future studies and encourage change in clinical care to decrease the occurrence of ARDS in surgical patients.

Enrollment

89 patients

Sex

All

Ages

11+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ARDS
  • post-surgical
  • ventilator

Exclusion criteria

  • rib fracture
  • pneumonia
  • sepsis

Trial design

89 participants in 2 patient groups

1
Description:
Control -- postoperative mechanical ventilation patients without ARDS
2
Description:
Cases -- postoperative mechanical ventilation patients with ARDS

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems