跳至主要内容
临床试验/NL-OMON26985
NL-OMON26985招募中不适用

Prospective cohort on pain after minimal-invasive ventral mesh rectopexy

Meander Medical Center, Amersfoort, The Netherlands0 个研究点目标入组 60 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
60

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

入选标准

  • Age = 18 years.
  • -Indication for ventral mesh rectopexy (VMR) set by the treating physician in accordance to the current guidelines on rectal prolapse.
  • -Counselled for therapeutic options and given informed consent for robot-assisted VMR (RVMR) or RVMR combined with sacrocolpopexy.
  • -Written informed consent for observational data collection.

排除标准

  • -Mentally incompetent patients (unable to fulfil questionnaires).
  • -A medical history of pelvic radiation therapy.
  • -Scheduled for a redo-rectopexy.
  • -A medical history of previously implanted pelvic floor meshes.

研究者

发起方
Meander Medical Center, Amersfoort, The Netherlands

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