跳至主要内容
临床试验/CTRI/2024/03/064111
CTRI/2024/03/064111尚未招募3 期

A randomised controlled trial to study the outcome of ‘Routine episiotomy’ versus ‘No episiotomy’ onperineal injury and pelvic floor dysfunction during normal vaginal delivery among primigravidawomen: A Pilot study - NI

AIIMS,0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
AIIMS,

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

  • Antenatal women with singleton cephalic presentation age 18 yrs to 40 yrs
  • Antenatal women admitted in the third trimester with singleton pregnancy having a cephalic presentation at more than 34 weeks who are expected to have a normal vaginal delivery

排除标准

  • 1. Any contraindication of vaginal delivery
  • 2. Pregnancies with multiple gestations
  • 3. Estimated fetal weight more than 3 Kg
  • 4. Previous surgery for incontinence and prolapse
  • 5. Women with bleeding disorders or anticoagulation
  • 6. Women with occipito posterior position.

研究者

发起方
AIIMS,

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