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Clinical Trial

A Post-Marketing Study of Alexa Medium for Сorrection of the Lips Volume Loss

NCT: NCT06961305 · COMPLETED

NCT IDNCT06961305
StatusCOMPLETED
Start Date2021-08-10
Completion2022-06-02

Brief Summary

This post-marketing, prospective, multicentre, single-arm, open-label clinical investigation aimed to evaluate the safety, tolerability, and effectiveness of the injectable medical device Alexa Medium (based on cross-linked hyaluronic acid) for the correction of lip volume loss. Participants received one or two injections of the product, and effectiveness was assessed using the Global Aesthetic Improvement Scale (GAIS) and the Medicis Lip Fullness Scale (MLFS). Safety data were collected at each visit. The study demonstrated high effectiveness and safety, with most subjects achieving their personal aesthetic goals.

Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.

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