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Clinical Trial Summary

Patients with a primary complaint of vaginal looseness and sexual dysfunction, visiting a sexual dysfunction clinic at a tertiary medical center will undergo randomization to either a series of 3 laser treatments or 3 sham treatments, and the effect of these treatments will be measured by several validated questionaires and by means of gynecological examination.


Clinical Trial Description

Patients suffering from vaginal looseness and sexual dysfunction, as a primary sexual dysfunction complaint will be recruited, sign an informed consent and will receive a thorough explanation regarding the side effects and possible beneficial affects the laser treatments may bestow. Patients will undergo randomization to either a series of 3 laser treatments or 3 sham treatments, and the effect of these treatments will be measured by several validated questionaires and by means of gynecological examination. Follow up after treatment cessation will be for 12 months post-treatment. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04228679
Study type Interventional
Source Rambam Health Care Campus
Contact
Status Completed
Phase N/A
Start date April 1, 2020
Completion date March 31, 2022

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