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Clinical Trial Summary

The ProACT Post Approval Study is a 5-year prospective, open-label, multi-center study designed to evaluate the long-term incidence of urethral stricture and device erosion after ProACT implantation. In addition, the study will evaluate whether treatment with ProACT affects clinical outcomes after subsequent SUI therapies.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03767595
Study type Interventional
Source Uromedica
Contact Patrick Gora
Phone 7636949880
Email pgora@uromedica-inc.com
Status Recruiting
Phase N/A
Start date February 19, 2019
Completion date September 1, 2030

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