Evaluation of Programs of Reeducation for Urinary Incontinence in Woman

Urinary Incontinence Clinical Trial

— ReedPerinee  

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02899520
• Other study ID #: 2014/09
• Secondary ID: 2014-A00709-38
• Status: Terminated
• Phase: N/A
• Start date: November 10, 2014
• Est. completion date: October 18, 2019

Study information

• Verified date: December 2019
• Source: Hopital Foch
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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)

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 60
• Est. completion date: October 18, 2019
• Est. primary completion date: October 18, 2019
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• 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

Exclusion Criteria:

• 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.

Related Conditions & MeSH terms

• Enuresis
• Urinary Incontinence

Intervention

Other:
• Reference method
Electrostimulation associated to perineal training
• CMP ® method
Method based on Knowledge and Control of Perineum

Locations

Country	Name	City	State
France	Hopital Foch	Suresnes

Sponsors (1)

Lead Sponsor	Collaborator
Hopital Foch

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	USP (Urinary Symptoms Profile) score	Urinary Symptoms Profile score	38 weeks