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Real-world Evidence Study on the Performance and Safety of Halova Ovules

Vaginal Atrophy Clinical Trial

Official title:
Real-world Evidence Study on the Performance and Safety of the Medical Device Halova Ovules in the Local Treatment of Vaginal Atrophy

Clinical Trial Summary

An open-label, multicentric, non-randomized, single-arm, pilot, interventional clinical investigation to confirm the tolerability and performance of the medical device Halova in lubrication of the vagina and vaginal atrophy treatment.

Clinical Trial Description

The primary objective of this investigation is to evaluate the therapeutic performance and tolerability of Halova ovules in treating vaginal atrophy and restoring the natural lubrication of the vaginal mucosa. The secondary objective of this clinical investigation are to evaluate the performance of the medical device by clinical examination, and the degree of patient satisfaction related to the intended use (Likert scale). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05654610
Study type Observational
Source Perfect Care Distribution
Contact
Status Completed
Phase
Start date March 1, 2022
Completion date July 31, 2022
View Details
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