Viveve Medical, Inc. announced that it has completed enrollment in its LIBERATE-International trial, a multicenter, randomized, double-blinded, sham-controlled study to evaluate the safety and efficacy of its proprietary, cryogen-cooled monopolar radiofrequency (CMRF) technology for the improvement of stress urinary incontinence (SUI) in women. This study is being conducted under an Investigational Testing Application which was approved by the Canadian Ministry of Health and by a central investigational review board. LIBERATE-International is a multicenter, randomized, double-blinded, and sham-controlled trial with an enrollment of approximately 100 subjects at up to ten study sites in Canada. Subjects are randomized in a 2:1 ratio for active and sham treatments. The primary efficacy endpoint is the mean change from baseline in the standardized 1-hour Pad Weight Test at six months post-treatment. The objective 1-hour Pad Weight Test is an FDA recommended endpoint for SUI clinical trials. The study design also includes multiple exploratory endpoints as well as safety follow-up throughout the study.