A Feasibility Study to Evaluate the Clinical Performance and Safety of the VITA AV Clinical System When Used for the Treatment of Vaginal Atrophy
Unknown Not Applicable NCT06207227
Study Description
The primary objective of this clinical investigation is to demonstrate that treatment with the VITA AV clinical system is feasible and to evaluate clinical performance and safety when used to improve the symptoms and signs of vaginal atrophy (VA) due to menopause.
Study Details
- Registry ID:
- NCT06207227
- Conditions:
- Vaginal Atrophy
- Phase:
- Not Applicable
- Target Enrollment:
- 12 participants
- Start Date:
- Age Range:
- 51–70 years
- Gender:
- Female
- Healthy Volunteers:
- No
Study Locations (1 site)
-
Pineo Clinic (Pineo Medical Ecosystem)
Tbilisi, Georgia
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