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Clinical Trial Summary

The study is intended to assess the safety and efficacy of CO2 AcuPulse laser treatment in patients with stress urinary incontinence (SUI). Eligible subjects will either receive 3 laser or sham treatment sessions, 4 weeks apart and 4 Follow Up visits, at 1, 3, 6, and 12 months following the last treatment.


Clinical Trial Description

Following a screening visit, eligible subjects will be enrolled into the study. Eligibility will be decided depending on the level of SUI the patient has. Each subject will receive either 3 laser or sham treatments 4 weeks apart and 4 Follow Up visits, at 1, 3, 6, and 12 months following the last treatment. Further demographic information and patient history will be obtained from the subjects' electronical files. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02861391
Study type Interventional
Source Rambam Health Care Campus
Contact
Status Completed
Phase N/A
Start date October 4, 2019
Completion date January 30, 2022

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