Status:
COMPLETED
Supplemental Perioperative Oxygen to Reduce the Incidence of Post-Cesarean Endometritis and Wound Infection
Lead Sponsor:
University of Washington
Conditions:
Wound Infection or Endometritis Post Cesarean Section
Eligibility:
FEMALE
16+ years
Phase:
NA
Brief Summary
The purpose of this study is to determine whether supplemental perioperative oxygen significantly decreases the incidence of post-Cesarean endometritis and wound infection among women who undergo Cesa...
Detailed Description
Women undergoing cesarean section after rupture of membranes or onset of labor are randomized in a one to one ratio to either normal or supplemental perioperative oxygen during cesarean section and fo...
Eligibility Criteria
Inclusion
- Women who underwent a clinically indicated cesarean delivery after the onset of labor or rupture of membranes
Exclusion
- Cesarean delivery prior to the onset of labor or rupture of membranes
- emergent cesarean delivery
- general endotracheal anesthesia
- clinical chorioamnionitis
- HIV infection
- less than 16 years of age
Key Trial Info
Start Date :
January 1 2001
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2006
Estimated Enrollment :
143 Patients enrolled
Trial Details
Trial ID
NCT00670020
Start Date
January 1 2001
End Date
December 1 2006
Last Update
May 1 2008
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