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临床试验/NCT01387685
NCT01387685撤回不适用

Treatment of Pelvic Organ Prolapse by PIVS Versus Surgeon Cut Mesh

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
主要终点
Satisfaction with study outcome

研究概览

简要总结

Women with pelvic floor prolapse who underwent surgery with mesh will be enrolled. The investigators will compare data from the chart, telephone interviews and physical examinations between those who underwent mesh placement to those who underwent placement of PIVS.

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 underwent surgery for pelvic floor prolapse

排除标准

  • Women who did not have surgery for pelvic floor prolapse.

结局指标

主要结局

Satisfaction with study outcome

时间窗: six to twelve months after surgery

次要结局

  • Side effects of the surgery: pain, vaginal erosion by tape, bleeding(Within six to twelve months after study)

研究者

申办方类型
Other Gov

研究点 (2)

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