跳至主要内容
临床试验/NCT06176521
NCT06176521已完成不适用

Evaluation of the Results of Laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Performed Without Mesh in the Surgical Treatment of Pelvic Organ Prolapse

Gaziosmanpasa Research and Education Hospital2 个研究点 分布在 2 个国家目标入组 35 人开始时间: 2023年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
35
试验地点
2
主要终点
Pre and post operative assessment of POP-Q measurements

研究概览

简要总结

Evaluation of the anatomical and functional results of laparoscopic sacrohysteropexy and sacrocolpopexy surgeries performed without using mesh in the surgical treatment of pelvic organ prolapse

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • being 18 years old or older
  • needing an operation for symptomatic pelvic organ prolapse -

排除标准

  • past history of chemotherapy or radiotherapy
  • past history of pelvic organ prolapse surgery
  • if there is a contraindication of laparoscopy -

结局指标

主要结局

Pre and post operative assessment of POP-Q measurements

时间窗: 1 year

POP-Q values of patients before and after laparoscopic Sacrohysteropexy and Sacrocolpopexy Surgeries Performed Without Mesh on Pelvic Organ Prolapse will be compared.

Pre and post operative assessment of Pelvic Organ Prolapse / Incontinence Sexual

时间窗: 1 year

Units on a scale of the patients obtained with Pelvic Organ Prolapse / Incontinence Sexual Questionnaire (PISQ-12) will be compared before and after surgery.

次要结局

未报告次要终点

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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