The Timing of Prophylactic Antibiotics in Cesarean Section and the Risk of Post-operative Febrile Morbidity
- Conditions
- Cesarean Section
- Registration Number
- NCT00133029
- Lead Sponsor
- University of Pennsylvania
- Brief Summary
The purpose of this study is to determine whether the timing of prophylactic antibiotic administration for cesarean section (immediate preoperative versus intraoperative administration) impacts the rate of postoperative febrile morbidity. The specific aim of the project is to test the hypothesis that preoperative antibiotic administration will decrease the rate of composite postoperative febrile morbidity.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- Female
- Target Recruitment
- Not specified
- Gestational age > 36 weeks
- Ability to understand requirements of the study
- Elective/non-emergent cesarean section selected as route of delivery by treating physicians
- Known fetal anomaly
- Exposure to antibiotics within 7 days of admission, including intrapartum group B streptococcal (GBS) prophylaxis
- Emergent cesarean delivery (i.e. for fetal distress, maternal distress, obstetric hemorrhage)
- Overt maternal intrapartum infection requiring antibiotics
- Prolonged rupture of membranes (>18 hours)
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
Hospital of the University of Pennsylvania
🇺🇸Philadelphia, Pennsylvania, United States
Hospital of the University of Pennsylvania🇺🇸Philadelphia, Pennsylvania, United States