Prospective, Open-Label, Single-Center, Non-Comparative Study to Assess

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.

See also
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Not yet recruiting	`NCT03238053` - Laser Treatment of Genito-urinary Syndrome in Women	N/A
Terminated	`NCT01753102` - Efficacy and Safety Of Spil's Estradiol Vaginal Tablet	Phase 3
Terminated	`NCT05627791` - Effects of Vaginal Oxytocin Gel on Vaginal Cytologic Parameters in Postmenopausal Woman	Phase 2/Phase 3

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

Prospective, Open-Label, Single-Center, Non-Comparative Study to Assess the Use of Pixel CO2 Laser System (FemiLift) in the Treatment of Vulvovaginal Atrophy (VVA) in Postmenopausal Female Subjects

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms