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临床试验/IRCT20181020041394N1
IRCT20181020041394N1招募中2 期

Effect of rectal Misoprostol in reducing blood loss before hysterectomy and myomectomy

Babol University of Medical Sciences0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
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
35 years 至 50 years(—)
性别
All

入选标准

  • Age between 35 and 50 years
  • The number of uterine fibroids is 5 or less
  • The maximum size of the largest fiber is 3 cm
  • All fibromas are subserosal or intramural in ultrasound
  • Uterus size less than 24 weeks pregnant with two-handed examination if need for myomectomy

排除标准

  • Any contraindication for using Misoprostol
  • The presence of malignancy
  • History of previous laparotomy except cesarean section
  • History of endometriosis
  • Cardiovascular and pulmonary diseases
  • Bleeding disorders
  • Hemoglobin below 10 g / dl
  • Body mass index greater than 30 kg / m²
  • Previous Myomectomy History
  • History of using misoprostol with GnRH immediately before surgery
  • Unwillingness to enter the study

研究者

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