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临床试验/ISRCTN64355848
ISRCTN64355848已完成不适用

Reducing blood loss in laparoscopic and open myomectomy: a prospective randomised controlled trial comparing the benefit of triple tourniquets against gonadotropin releasing hormone (GnRH) analogues

Record Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)0 个研究点目标入组 100 人开始时间: 2005年9月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
100

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

性别
Female

入选标准

  • Current inclusion criteria as of 15/09/2008:
  • Inclusion criteria for open myomectomy:
  • 1. Symptomatic multiple fibroids (more than three fibroids)
  • 2. Uterine size less than 24 weeks gestation equivalent
  • Inclusion criteria for laparoscopic myomectomy:
  • 1. Uterine size up to 16 - 18 weeks gestation equivalent
  • 2. No more than three fibroids, with maximum diameter of 15 cm 3. Mostly intramural fibroids
  • Initial inclusion criteria:
  • Patients will be referred from the GP to our fibroid clinic and have symptomatic fibroids. They will have chosen to have a myomectomy and agreed to be in the study.

排除标准

  • Added as of 15/09/2008:
  • Exclusion criteria for open myomectomy:
  • 1. Large uterus more than 24 weeks gestation equivalent
  • 2. Women with a bleeding disorder
  • 3. Women on anticoagulants
  • 4. Treatment with GnRH analogues within the previous six months
  • 5. Women with a haemoglobin level of less than 10.5 g/dl
  • Exclusion criteria for laparoscopic myomectomy:
  • 1. Uterine size of more than 16 - 18 weeks gestation equivalent
  • 2. Women with a bleeding disorder
  • 3. Women on anticoagulants
  • 4. Women with a haemoglobin level of less than 10.5 g/dl
  • 5. Mostly subserous fibroids

研究者

发起方
Record Provided by the NHSTCT Register - 2005 Update - Department of Health (UK)

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