NCT00330278已完成不适用
A Randomized, Double-Blind, Placebo Controlled Trial of Cefazolin Given Either 30 Minutes Prior to Cesarean Section or at Cord Clamping
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 350
- 试验地点
- 2
- 主要终点
- Combined infectious morbidity - endometritis + wound infection
研究概览
简要总结
This is a randomized, double-blinded placebo controlled trial of cefazolin timing before cesarean section fo infection prophylaxis. Subjects are randomized to cefazolin either 30 minutes prior to skin incision or at time of cord-clamping. Primary outcome is infectious morbidity including wound infections and endometritis.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Double
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Pregnant 24-43 weeks gestation > 18 years old Requiring cesarean section -
排除标准
- •Receiving antibiotics < 18 years old Allergy to cefazolin
结局指标
主要结局
Combined infectious morbidity - endometritis + wound infection
次要结局
- Neonatal sepsis
- Allergic reactions
研究者
研究点 (2)
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