Stress Urinary Incontinence Clinical Trial
Official title:
Pilot Single-masked, Randomized, 3-arm Parallel Study Assessing the Tolerability, Safety and Efficacy of Intraurethral/Intravaginal 2940 nm Er:YAG Laser Treatment For Stress Urinary Incontinence
Primary objective is to assess the tolerability and safety of the intraurethral 2940nm Er:YAG laser technique in combination with intravaginal 2940nm Er:YAG laser method for the treatment of stress urinary incontinence.
This study is a prospective, randomized, 3-arm parallel pilot study. Study subjects will be
women currently experiencing female stress urinary incontinence (SUI) and stress-predominant
mixed urinary incontinence (SMUI) with a degree of intrinsic sphincter deficiency for a
minimum duration of 6 months prior to enrolment. Diagnosis of SUI with a degree of intrinsic
sphincter deficiency will be performed using urodynamic and clinical assessment.
Subjects will undergo sham, intravaginal, and the combination of intravaginal and
intraurethral treatment with the 2940 nm Er:yttrium aluminum garnet Er:YAG laser at two time
points, 4 weeks apart. Primary objective is to assess the tolerability and safety of the
intraurethral 2940nm Er:YAG laser technique in combination with intravaginal 2940nm Er:YAG
laser method for the treatment of stress urinary incontinence through 6 months follow-up and
extend to 12 months follow-up.
Secondary objective is to assess the effectiveness of the intravaginal and combination of
intraurethral/intravaginal laser treatments using subjective and objective measures, as well
as improvement in quality of life through 6 months follow-up and extend to 12 months
follow-up.
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