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The Effect of Forced Air Warming During Cesarean Section on Postoperative Infectious Morbidity

NCT00696462 · Status: WITHDRAWN · Phase: NA · Type: INTERVENTIONAL

Last updated 2012-09-13

No results posted yet for this study

Summary

The purpose of this study will be to assess whether forced air warming decreases the rate of surgical site infections following cesarean section.

Conditions

  • Cesarean Section

Interventions

DEVICE

forced-air warming

forced-air warming device

Sponsors & Collaborators

  • Vanderbilt University

    lead OTHER

Principal Investigators

  • Curtis L Baysinger, M.D. · Vanderbilt University Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-03-31
Primary Completion
2009-04-30
Completion
2009-04-30

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 NCT00696462 on ClinicalTrials.gov