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Clinical Trial Summary

The study is intended to assess the safety and efficacy of Carbon dioxide AcuPulse laser treatment in patients with stress urinary incontinence. Eligible subjects will be randomized to either receive 3 laser or 3 sham treatment sessions, 4 weeks apart and 3 follow up visits 3, 6 and 12 months following the last treatment.


Clinical Trial Description

Following a screening visit, eligible subjects will be enrolled into the study. Subjects will be randomized into either laser treatment or sham treatment. Each subject will receive 3 treatments 4 weeks apart and 3 follow up visits, at 3, 6 and 12 months following the last treatment. Further demographic information and patient history will be obtained from the subjects' electronic files. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05097456
Study type Interventional
Source Rambam Health Care Campus
Contact
Status Completed
Phase N/A
Start date March 1, 2020
Completion date December 31, 2021

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