跳至主要内容
临床试验/PACTR202308561344907
PACTR202308561344907招募中Unknown

Peri-operative vaginal cleansing using 4% chlorhexidine versus 10% povidone-iodine solution to prevent post-caesarean endometritis in Ilorin: A randomized controlled study

Self0 个研究点目标入组 136 人开始时间: 2023年7月10日最近更新:
适应症

试验速览

阶段
Unknown
状态
招募中
发起方
Self
入组人数
136

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

  • Women aged =18 years scheduled for non-elective CS irrespective of the booking status.
  • Live intrauterine fetus (es).
  • Consent to participate in the study

排除标准

  • Active genital warts.
  • Women with antepartum haemorrhage or an ongoing episode of vaginal bleeding.
  • Reported allergy to chlorhexidine and / or iodine containing solution.
  • Women previously on antibiotic therapy for more than 24hours before surgery irrespective of the indication.
  • Women with fetus (es) with face presentation.
  • Women with clinical diagnosis of chorioamionitis..
  • Women with diagnosed thyroid disorders or goitre on examination.

研究者

发起方
Self

相似试验