Last updated on March 2020

ProACT Post-Approval Study

Brief description of study

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 Study Identifier: NCT03767595

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Emory University

Atlanta, GA United States
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University of Michigan

Ann Arbor, MI United States
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