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临床试验/PACTR202310568262804
PACTR202310568262804已完成Unknown

Comparison of combined misoprostol and oxytocin with oxytocin alone in the control of blood loss during elective caesarean section.

未提供0 个研究点目标入组 174 人开始时间: 2023年9月27日最近更新:

试验速览

阶段
Unknown
状态
已完成
入组人数
174

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

  • Consenting women with term pregnancies undergoing elective lower segment caesarean delivery under spinal anaesthesia.

排除标准

  • Women with predisposing factors for PPH, such as;
  • Multiple gestations,
  • Placenta praevia,
  • Undiagnosed vaginal bleeding, were excluded from the study.
  • Patients who had general anaesthesia
  • Patients with surgical indications requiring general anaesthesia, cardiovascular, renal, or hepatic dysfunction.
  • Patients who presented with fever or refused to give consent were excluded.

研究者

发起方
未提供

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