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临床试验/ACTRN12605000182695
ACTRN12605000182695招募中未知

The measurement of urethral pressure with the MoniTORR* device to predict outcome after urinary incontinence surgery based on urodynamics studies at 6 months.

Johnson & Johnson Medical0 个研究点目标入组 120 人开始时间: 2005年8月19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
120

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

年龄范围
ot stated 至 ot stated(—)
性别
All

入选标准

  • Women with urodynamics stress incontinence undergoing a TVT procedure at the two study centres. Concomitant prolapse surgery is not a contraindication. Willingness to participate.

排除标准

  • Medically unfit for surgery. Refusal to participate. Patients who are recommended surgery other than TVT (e.g. Colposuspension, Sling, Bulking agent, Transobturator procedure).

研究者

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