Uterine Flora During Elective and Urgent Cesarean Sections
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|ClinicalTrials.gov Identifier: NCT00500019|
Recruitment Status : Completed
First Posted : July 12, 2007
Last Update Posted : March 31, 2009
|Condition or disease|
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.
|Study Type :||Observational|
|Estimated Enrollment :||600 participants|
|Official Title:||Uterine Flora During Elective and Urgent Cesarean Sections and Its Relationship to Postpartum Complications.|
|Study Start Date :||January 2005|
|Actual Study Completion Date :||September 2008|
Elective Cesarean sections
Non-elective cesarean section
- To compare bacteriological growth between elective and non-elective cesarean section [ Time Frame: 5 years ]
- To study the various bacteria growth in the uteri, and to compare type of bacteria to post-op morbidity [ Time Frame: 5 years ]
Biospecimen Retention: Samples Without DNA
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00500019
|Western Galilee Hospital|
|Nahariya, Israel, 22100|
|Principal Investigator:||Ido Solt, MD||Western Galilee Hospital|