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Carbon Dioxide Acupulse Laser Treatment Versus Sham Treatment and Sexual Dysfunction.

Sexual Dysfunction Clinical Trial

Official title:
Randomized, Double-blind, Sham-controlled Clinical Trial for Evaluating the Efficacy of Fractional Carbon Dioxide Laser in the Treatment of Female Sexual Dysfunction.

Clinical Trial Summary

The study is intended to assess the safety and efficacy of Carbon dioxide AcuPulse laser treatment in patients with sexual dysfunction. 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

Clinical Trial Details
NCT number NCT05097469
Study type Interventional
Source Rambam Health Care Campus
Contact Roy Lauterbach, MD
Phone +972-52-9432416
Email r_lauterbach@rambam.health.gov.il
Status Recruiting
Phase N/A
Start date October 4, 2021
Completion date November 30, 2023
View Details
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