NCT00656071

Brief 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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
89

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Oct 2007

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2007

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

April 4, 2008

Completed
6 days until next milestone

First Posted

Study publicly available on registry

April 10, 2008

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2008

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2008

Completed
Last Updated

September 7, 2012

Status Verified

September 1, 2012

Enrollment Period

10 months

First QC Date

April 4, 2008

Last Update Submit

September 5, 2012

Conditions

Keywords

ARDSAcute respiratory distress syndromeAdult respiratory distress syndromerespiratory distress

Outcome Measures

Primary Outcomes (1)

  • ARDS

    data pulled from 10/2000 - 08/2007

Study Arms (2)

1

Control -- postoperative mechanical ventilation patients without ARDS

2

Cases -- postoperative mechanical ventilation patients with ARDS

Eligibility Criteria

Age11 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The surgical and post-op patients at VUMC. The collection dates will be from October 1, 2001 until August 31, 2007.

You may qualify if:

  • ARDS
  • post-surgical
  • ventilator

You may not qualify if:

  • rib fracture
  • pneumonia
  • sepsis

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Vanderbilt University Medical Center

Nashville, Tennessee, 37212, United States

Location

Related Links

MeSH Terms

Conditions

Respiratory Distress SyndromeDyspnea

Condition Hierarchy (Ancestors)

Lung DiseasesRespiratory Tract DiseasesRespiration DisordersSigns and Symptoms, RespiratorySigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Christopher G Hughes, M.D.

    Vanderbilt University Medical Center

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assistant Professor

Study Record Dates

First Submitted

April 4, 2008

First Posted

April 10, 2008

Study Start

October 1, 2007

Primary Completion

August 1, 2008

Study Completion

August 1, 2008

Last Updated

September 7, 2012

Record last verified: 2012-09

Locations