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临床试验/ISRCTN33435996
ISRCTN33435996已完成未知

Vaginal Preparation at caesarean section to Reduce Endometritis and Prevent Sepsis – a feasibility study of chlorhexidine gluconate

Birmingham Children's Hospital0 个研究点目标入组 250 人开始时间: 2017年8月14日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
250

研究概览

简要总结

2018 protocol in: https://www.ncbi.nlm.nih.gov/pubmed/29881638 2019 qualiative study results in: https://www.ncbi.nlm.nih.gov/pubmed/31307417 (added 17/07/2019)

研究设计

研究类型
Interventional

入排标准

性别
Female

入选标准

  • 1. Women greater than or equal to 34 weeks pregnant having an elective or emergency CS, regardless of indication
  • 2. Women aged 16 years and over
  • 3. Women carrying singletons and all higher order multiples

排除标准

  • 1. Any women with a known allergy to chlorhexidine gluconate or any of its ingredients
  • 2. Unable to give informed consent
  • 3. Unable to receive a telephone interview at 6 weeks post natal
  • 4. Preterm delivery less than 34 weeks
  • 5. Receiving intrapartum antibiotics for GBS prophylaxis or suspected infection in labour

研究者

发起方
Birmingham Children's Hospital

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