Protocol Number: U9915 – Solyx vs. Obtryx 08/2013 - Present
Title: A Prospective, Non-Randomized, Parallel Cohort, Multi-center Study of the SolyxTM Single Incision Sling System vs. the ObtryxTM II Sling System for the Treatment of Women with Stress Urinary Incontinence
Purpose of Study
The purpose of this research study is to compare the treatment device (Solyx) to a different mesh sling or control device (Obtryx II) for the treatment of symptoms for SUI. Safety information and patient outcomes will be collected for three (3) years and evaluated.