Effect of BTL-899 Device for Non-invasive Lipolysis on Human Upper Arms

Status Completed

Clinical Trial Summary

This study will evaluate the clinical safety and the performance of the BTL-899 device during the treatment of upper arms.

Clinical Trial Description

The aim of the study is to confirm the efficacy and the safety of the treatment. The efficacy (reduction of excess adipose tissue) will be assessed via correct identification of pre-treatment and 3-months follow-up images by at least two out of three independent blinded evaluators. The fat reduction will be also measured by means of ultrasound. Comfort and satisfaction will be assessed via standard questionnaires. Safety measures will include documentation of adverse events (AE) during and after the procedures. ;

Study Design

Related Conditions & MeSH terms

Fat Burn

Clinical Trial Details

NCT number	NCT04643275
Study type	Interventional
Source	BTL Industries Ltd.
Contact
Status	Completed
Phase	N/A
Start date	October 15, 2020
Completion date	September 2, 2021

View Details

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