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临床试验/ACTRN12615000427572
ACTRN12615000427572已完成不适用

Comparative study of laparoscopic versus abdominal sacral colpopexy in women with Grade III or IV uterovaginal prolapse evaluating operating room time, estimated blood loss , inpatient days, and recurrence

alexandria university, faculty of medicne0 个研究点目标入组 30 人开始时间: 2015年5月5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
30

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment

入排标准

年龄范围
30 Years 至 80 Years(—)
性别
Female

入选标准

  • 1.Grade III or IV uterovaginal prolapse according to the pelvic organ prolapse quantification (POP-Q).
  • 2.Uterine or vault prolapse .
  • 3.Normal uterus and ovaries on ultrasound examination.
  • 4.Normal menstrual bleeding pattern (if premenopausal).
  • 5.Normal Pap smear.

排除标准

  • 1.Inability to give informed consent or to return for follows up.
  • 2.Unable to undergo general anaesthesia.
  • 3.Prior sacral colpopexy.
  • 4.Patients presenting with lower grade prolapse.
  • 5.Genuine stress incontinence.
  • 6.Indication for hysterectomy

研究者

发起方
alexandria university, faculty of medicne

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