The Timing of Prophylactic Antibiotics in Cesarean Section and the Risk of Post-operative Febrile Morbidity

Phase 4TerminatedNCT00133029

University of Pennsylvania

Overview

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.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Masking

NONE

Conditions

Cesarean Section

Interventions

Timing of prophylactic antibiotic administrationDRUG

Eligibility

Sex: FEMALE

Medical Language ↔ Plain English

Inclusion Criteria: * Gestational age \> 36 weeks * Ability to understand requirements of the study * Elective/non-emergent cesarean section selected as route of delivery by treating physicians Exclusion Criteria: * 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)

Locations (1)

Hospital of the University of Pennsylvania

Philadelphia, Pennsylvania, United States

Data from ClinicalTrials.gov

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