Uterine Flora During Elective and Urgent Cesarean Sections
NCT ID: NCT00500019
Last Updated: 2009-03-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
600 participants
OBSERVATIONAL
2005-01-31
2008-09-30
Brief Summary
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Detailed Description
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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
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Study Design
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PROSPECTIVE
Study Groups
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1.
Elective Cesarean sections
No interventions assigned to this group
2.
Non-elective cesarean section
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
50 Years
FEMALE
Yes
Sponsors
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Western Galilee Hospital-Nahariya
OTHER_GOV
Responsible Party
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Department Obstetrics & Gynecology, Western Galilee Hospital, Nahariya, Israel
Principal Investigators
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Ido Solt, MD
Role: PRINCIPAL_INVESTIGATOR
Western Galilee Hospital
Locations
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Western Galilee Hospital
Nahariya, , Israel
Countries
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Other Identifiers
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1-Bornstein
Identifier Type: -
Identifier Source: org_study_id