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临床试验/NCT01383291
NCT01383291撤回不适用

Postoperative Comparison Between Posterior Prolift Mesh Placement and Posterior IVS Sling Placement

Western Galilee Hospital-Nahariya2 个研究点 分布在 1 个国家开始时间: 2009年2月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
2

研究概览

简要总结

  • Women who underwent mesh or sling procedures to correct pelvic organ prolapse will be enrolled.
  • Their data will be collected from the files.
  • Comparison between two groups will be carried our: Those who underwent a posterior IVS and those who underwent posterior prolift procedure.
  • The data will be obtained by questionaires by a telephone interview by a physician who did not participate in the surgery.
  • Follow-up physical examination data will also be obtained.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 95 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Women who previously underwent surgery for pelvic floor prolapse at least a year before

排除标准

  • Women who did not have surgery for pelvic floor prolapse

研究者

申办方类型
Other Gov

研究点 (2)

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