NCT00762593

Trial Evaluating Transvaginal Electrical Stimulation With a Home Use Programmable Device for Urinary Stress Incontinence

A Multicenter Double Blind Randomized Placebo Controlled Trial Evaluating Transvaginal Electrical Stimulation With a Home Use Programmable Device for Urinary Stress Incontinence

• Status: Unknown
• Phase: Phase 2
• Study type: Interventional
• Enrollment: 150 (actual)
• Sponsor: Akontis · Industry
• Sex: Female
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

To compare the effectiveness of a transvaginal electrical stimulation by a home use programmable device to a placebo device for urinary incontinence in women

Conditions

• Urinary Stress Incontinence

Interventions

Type	Name	Description
DEVICE	transvaginal placebo device	Use of a transvaginal placebo home use programmable device used 30 minutes every day during 8 weeks
DEVICE	transvaginal electrical stimulation device	Use of a transvaginal electrical stimulation home use programmable device used 30 minutes every day during 8 weeks

Timeline

• Start date: 2006-01-01
• Primary completion: 2008-10-01
• Completion: 2008-10-01
• First posted: 2008-09-30
• Last updated: 2008-10-17

Locations

1 site across 1 country: France