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临床试验/PACTR201802003039106
PACTR201802003039106已完成未知

Comparing Perioperative Vaginal Misoprostol With Intraoperative Pericervical Haemostatic Tourniquet In Reducing Blood Loss During Abdominal Myomectomy

niversity of Ilorin Teaching Hospital0 个研究点目标入组 80 人开始时间: 2018年2月2日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
80

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
20 Year(s) 至 48 Year(s)(—)
性别
Female

入选标准

  • Diagnosis of uterine fibroid with a treatment plan for abdominal myomectomy

排除标准

  • 1.Known allergy to prostaglandins including misoprostol.
  • 2.Chronic medical disorders including hypertension, diabetes mellitus, cardiac or pulmonary diseases.
  • 3.Previous uterine surgery (myomectomy or caesarean section).
  • 4.Known bleeding or clotting disorders.
  • 5.Haematocrit at 24hours before surgery less than 30%.
  • 6.Patient refusal to participate in the study.

研究者

发起方
niversity of Ilorin Teaching Hospital

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