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BTL-785F Device for Non-invasive Treatment of Wrinkles and Improvement of the Face Appearance

Wrinkle Clinical Trial

Official title:
Evaluation of Safety and Efficacy of the BTL-785F Device for Non-invasive Reduction of Wrinkles and Overall Improvement of Appearance of the Face

Clinical Trial Summary

This study will evaluate the clinical safety and the performance of the BTL-785F system equipped with the BTL-785-7 applicator for non-invasive treatment of facial wrinkles.

Clinical Trial Description

The study is a multicenter single-arm, open-label, interventional study. The subjects will be enrolled and assigned into one experimental study arm. The subjects will be required to complete four (4) treatment visits and two follow-up visits. At the baseline visit health status will be assessed and, if needed, additional tests will be performed. Inclusion and exclusion criteria will be verified and informed consent will be signed. The treatment administration phase consists of four (4) treatment visits, delivered 5-10 days apart. Safety measures will include documentation of adverse events (AE) including the subject's experience of pain or discomfort after the procedure. Occurence of AE's will be checked immediately after the first treatment visit, prior/post to the every other procedure and at the follow-ups. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05524805
Study type Interventional
Source BTL Industries Ltd.
Contact
Status Recruiting
Phase N/A
Start date June 6, 2022
Completion date February 2023
View Details
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