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Clinical Trial Summary

The purpose of this study is to assess the use of the Alma CO2 Pixel FemiLift™ in the treatment of VulvoVaginal Atrophy (VVA) in postmenopausal female subjects. The primary endpoint is to assess the change in the vaginal dryness by means of a Visual Analogic Scale (10 cm VAS) and/or Bachmann Index in VVA. The clinical improvement will be assessed by patient filled Vulvovaginal Atrophy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02747641
Study type Interventional
Source Alma Lasers Inc.
Contact
Status Completed
Phase N/A
Start date May 2016
Completion date August 2017

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