Treatment of Vaginal Atrophy With Low Intensity Nanosecond Neodymium Laser
Recruiting
N/A
Interventional Study
Postmenopausal Period
Vaginal Atrophy
Vaginal Prolapse
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
At a Glance
- Age
- 40 – 75
- Sex
- Female
- Study type
- Interventional
- Purpose
- Supportive Care
- Participants needed
- 120 (estimated)
- Sponsor
- MeLSyTech, Ltd · Industry
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About This Trial
The aim of study is characteristic of changes in the vaginal wall after treatment of neodymium laser radiation with a wavelength of 1064 nm. To assess the condition of the vaginal walls before and after laser treatment, the following methods will be used: vaginal health index, perineometry, measurement of the vaginal wall thickness by ultrasound, Doppler sonography of the vaginal walls vessels, op…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Age of 40-75 years, inclusive;
* Vaginal atrophy or 1st grade vaginal prolapse with atrophy, or lack of vaginal atrophy in case of control group 2;
* All participants have informed consent to conduct a course of procedures according to protocol, carry out follow-up visits, and…
Contacts