跳至主要内容
临床试验/PACTR202308564052985
PACTR202308564052985尚未招募Unknown

Optimal duration of bladder catheterization after elective caesarean section to prevent urinary tract morbidity: a randomized controlled trial of 12 versus 24 hours.

Dr Loretta Nnakwe0 个研究点目标入组 104 人开始时间: 2023年8月8日最近更新:
适应症

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
104

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

  • Pregnant women scheduled for elective caesarean section at term.
  • Elective caesarean section done under spinal anaesthesia
  • Participants who gave consent for the study
  • Participants with no pre-operative clinical evidence of urinary tract infection.

排除标准

  • Pregnant women whose condition require emergency caesarean section.
  • Elective caesarean section done under general or epidural anaesthesia
  • Pregnant women who did not give consent for the study.
  • Participants who withdrew their consent in the course of the study.
  • Pregnant women with pre-operative clinical evidence of urinary tract infection.
  • Participants with intra-operative bladder injury.
  • Pregnant women with medical condition like cardiac, renal or liver disease.
  • Pregnant women with retroviral disease.

研究者

发起方
Dr Loretta Nnakwe

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