Clinical Trials Directory

Trials / Completed

CompletedNCT00500019

Uterine Flora During Elective and Urgent Cesarean Sections

Uterine Flora During Elective and Urgent Cesarean Sections and Its Relationship to Postpartum Complications.

Status
Completed
Phase
Study type
Observational
Enrollment
600 (estimated)
Sponsor
Western Galilee Hospital-Nahariya · Other Government
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

Hypothesis: The bacterial flora of the uterus during elective Cesarean sections differs from the uterine flora during non-elective Cesarean sections. We want to study whether the uterine flora can predict post-cesarean febrile morbidity and endometritis.

Detailed description

Objective: To evaluate the uterine flora at the time of elective and non-elective cesarean sections and to study the relationship to the development of postpartum fever and/or endometritis. Methods: Eight-hundred women who will be delivered by cesarean section will be enrolled in this study. Cultures will be obtained during the surgery from the open uterine cavity after removal of the placenta. Data regarding postpartum morbidity would be collected.

Conditions

Timeline

Start date
2005-01-01
Completion
2008-09-01
First posted
2007-07-12
Last updated
2009-03-31

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT00500019. Inclusion in this directory is not an endorsement.