NCT02126228已完成不适用
A Randomized Controlled Trial on Antibiotics Application For Low Infection-risked Elective Cesarean
Fanzhen Hong1 个研究点 分布在 1 个国家目标入组 212 人开始时间: 2012年11月最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 212
- 试验地点
- 1
- 主要终点
- Temperature
研究概览
简要总结
The purpose of this study is to discuss whether the parturients who underwent elective cesarean of such kind do not need prophylactic use of antibiotics and evaluate the risks and economic benefits involved.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
入排标准
- 年龄范围
- 20 Years 至 45 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Elective cesarean
- •With normal temperature;
- •No signs of infection;
- •Normal degree of cleanliness in vaginal; .Normal amniotic fluid.
排除标准
- •Failure of vaginal delivery and emergency cesarean;
- •Premature rupture of membranes;
- •Antibiotics having been applied to 3 days before cesarean;
- •Having inflammation before cesarean: such as vaginitis, pelvic inflammatory disease, chorioamnionitis;
- •Having infections in respiratory or urinary system before cesarean;
- •Placenta previa or placental abruption;
- •With medical and surgical complications;
- •BMI ≥ 30kg/m2;
- •Total blood loss more than 1000ml within 2 hours after cesarean
结局指标
主要结局
Temperature
时间窗: 3days
次要结局
- Postpartum hemorrhage volume estimates and Routine blood test.(3days)
研究者
Fanzhen Hong
Obstetrics of 2nd Hopital
Shandong University
研究点 (1)
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