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
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