Evaluation of the Safety and Efficacy of Carbon Dioxide (CO2) Acupulse Laser Treatment on Urinary Stress Incontinence.

Exposure Laser Clinical Trial

Official title: Evaluation of the Safety and Efficacy of CO2 Acupulse Laser Treatment on Women With Urinary Stress Incontinence.

Status Completed

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. ;

Related Conditions & MeSH terms

• Exposure Laser
• Urinary Incontinence, Stress

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