NCT00133029终止4 期
The Timing of Prophylactic Antibiotics in Cesarean Section and the Risk of Post-operative Febrile Morbidity
适应症
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 终止
- 试验地点
- 2
研究概览
简要总结
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 盲法
- None
入排标准
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Gestational age > 36 weeks
- •Ability to understand requirements of the study
- •Elective/non-emergent cesarean section selected as route of delivery by treating physicians
排除标准
- •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)
研究者
研究点 (2)
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