Efficacy and safety of a novel disposable intravaginal device for treating stress urinary incontinence

Objective The purpose of this study was to evaluate the efficacy and safety of a novel disposable intravaginal device for treatment of stress urinary incontinence (SUI) in women. Study Design Sixty women with severe SUI were recruited from 2 sites in Israel to wear preweighed pads during a 7-day control period followed by a 28-day device usage period in which the device and preweighed pads were worn daily for 8 hours. The primary endpoint was the percentage of women who achieved a ≥ 70% reduction in pad weight gain (PWG) from the control period to the last 14 days of device usage. Results Sixty women who enrolled into the study and used the device for any period of time were included in the intent to treat (ITT) population. Eighty-five percent of them achieved a ≥ 70% reduction in PWG ( P = .01). Improvements in overall quality of life, subjective perception of incontinence, and satisfaction with the device were observed. Conclusion The intravaginal device is easy to use, well-tolerated, and effective in reducing SUI.