跳至主要内容
临床试验/CTRI/2021/10/037302
CTRI/2021/10/037302已完成未知

To compare the rate of cesarean section with the use of new WHO partograph and the old WHO partograph - A randomized controlled trial

AIIMS Jodhpur0 个研究点目标入组 570 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
AIIMS Jodhpur
入组人数
570

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

入选标准

  • All pregnant women (both primigravida and multigravida) with singleton pregnancy at >36 weeks gestation admitted for vaginal delivery.

排除标准

  • 1.Women admitted for elective LSCS.
  • 2.Women with multifetal pregnancy.
  • 3.Women with malpresentation.
  • 4.Women with h/o uterine surgery eg: cesarean section, myomectomy etc.
  • 5.Women with contracted pelvis or cephalopelvic disproportion.
  • 6.Patients not giving consent

研究者

发起方
AIIMS Jodhpur

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