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临床试验/NCT02899520
NCT02899520终止不适用

Evaluation of Programs of Reeducation for Urinary Incontinence in Woman

Hopital Foch2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2014年11月10日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
发起方
Hopital Foch
入组人数
60
试验地点
2
主要终点
USP (Urinary Symptoms Profile) score

研究概览

简要总结

The objective of this study is to compare two methods of pelvic floor muscle training: reference method versus CMP ® method ( (Connaissance et Maîtrise de Périnée : Knowledge and Control of Perineum)

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Patients more than 18 years old and less than 75 years
  • Patients presenting an urinary incontinence of effort or mixed symptomatic associated with a pelvic statics disorder
  • Patients with a perineale reeducation prescription
  • Patients affiliated to a national insurance scheme or benefiting from such a program
  • Patients having given her written consent form

排除标准

  • Nulliparous woman
  • Patients already operated for their incontinence
  • Patients with a prolapse of higher level at the stage II of the classification POP-Q (Pelvic Organ Prolapse Quantification)
  • Pregnant women
  • Patients presenting an associated anal incontinence,
  • Patients presenting a cancellation (section of marrow, syringomyelia for example) or an inversion of perineum control
  • Patients having given birth less than 6 months before the care
  • Patients having benefited from a pelvi-périnéale reeducation in the previous 12 months,
  • Patients presenting psychiatric disease
  • Patients presenting a vaginismus,
  • Patients presenting a contraindication to the practice of the electrostimulation.

结局指标

主要结局

USP (Urinary Symptoms Profile) score

时间窗: 38 weeks

Urinary Symptoms Profile score

次要结局

未报告次要终点

研究者

发起方
Hopital Foch
申办方类型
Other
责任方
Sponsor

研究点 (2)

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