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临床试验/CTRI/2021/03/032275
CTRI/2021/03/032275尚未招募4 期

To study efficay of sublingual Misoprostol vs intravenous Tranexamic acid in reducing amount of blood loss in full term pregnant women undergoing primary LSCS :A randomized control trial

Aarupadi Veedu Medical College and Hoppital0 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
4 期
状态
尚未招募
发起方

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

  • Full term women undergoing primary Cesarean Section at Aarupadi Veedu Medical College and Hospital who are willing to participate

排除标准

  • 1)Previous Cesarean Section
  • 2)Induced/augmented labour
  • 4)chorioamnionitis
  • 5)antepartum hemorrhage
  • 6)pre term pregnancy
  • 7)overdistension-multipregnancy,polyhydromnios

研究者

发起方
Aarupadi Veedu Medical College and Hoppital

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