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Clinical Trial Summary

This open-label proof-of-concept study is designed to evaluate the impact of the leva digital incontinence system on the treatment of stress and mixed urinary incontinence in women over a six week period. Subjects will participate in a 2.5 minute exercise program twice daily (performed at a clinic with therapist assistance 5x weekly, and at home once daily on weekdays and twice daily on weekends. Validated surveys (UDI-6, IIQ-7 and PGI-I) will be used to evaluate symptom relief. A battery of pelvic floor muscle exercises will be performed weekly to evaluate progress in muscle strengthening.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03536923
Study type Interventional
Source Renovia, Inc.
Contact
Status Completed
Phase N/A
Start date April 10, 2017
Completion date October 20, 2017

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