Fat Burn Clinical Trial
Official title:
Effect of BTL-899 Device for Non-invasive Lipolysis on Human Upper Arms
This study will evaluate the clinical safety and the performance of the BTL-899 device during the treatment of upper arms.
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. ;
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