跳至主要内容
临床试验/PACTR202201669178899
PACTR202201669178899已完成3 期

Effectiveness of Chlorhexidine vaginal cleansing in reducing postcaesarean surgical site infection and endometritis at two tertiary hospitals in Enugu, Nigeria: a randomized controlled trial

未提供0 个研究点目标入组 510 人开始时间: 2022年1月3日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
510

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19 Year(s) 至 44 Year(s)(—)
性别
Female

入选标准

  • All pregnant women who had been billed for caesarean delivery either electively or as emergency and given consent at the two Obstetrics units (ANW and Labour wards) of the two study centers were included

排除标准

  • women with clinical diagnosis of chorioamnionitis
  • women with diagnosis of obstructed labour
  • women with contraindications to caesarean delivery
  • women with contraindication to chlorhexidine use such as history of serious allergic reaction
  • women with premature rupture of membranes, HIV/AIDs, diabetes mellitus and hemoglobin <10g/dl that could not be corrected before surgery

研究者

发起方
未提供

相似试验