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临床试验/ACTRN12622000830796
ACTRN12622000830796招募中未知

A prospective cohort study for success of vaginal hysterectomy with vault suspension compared to Manchester-Fothergill Procedure for utero-vaginal prolapse

Mercy Hospital0 个研究点目标入组 202 人开始时间: 2022年6月14日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
入组人数
202

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
Non-randomised trial
主要目的
Treatment
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 80 Years(—)
性别
Female

入选标准

  • Inclusion Criteria
  • All participants between the ages of 18-80 with symptomatic stage I-III pelvic organ prolapse (POP) requesting surgery including hysterectomy, capable of providing informed consent and able to return for follow up.

排除标准

  • Exclusion Criteria
  • Any previous prolapse surgery
  • Previous surgery in the treatment area in the last year.
  • Systemic steroids use within the last 3 months
  • Pelvic organ prolapse (POP) > stage 3 according to pelvic organ prolapse quantification system
  • Past history of prolapse surgery with transvaginal mesh
  • Serious systemic disease or any chronic condition that could interfere with study compliance
  • Uterine pathology that would make uterine preservation inappropriate
  • Co-morbidities or surgical history that would make a particular approach inappropriate
  • Any other reason that, in the opinion of the investigator, prevents the subject from participating in the study or compromise the subject safety

研究者

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