Effect of the BTL-899 Therapy for Non-invasive Lipolysis and Circumference Reduction of Abdomen When Compared to a Sham Treatment

Improvement of Abdomen Appearance Clinical Trial

Official title: Evaluation of Safety and Efficacy of the BTL-899 Device for Non-invasive Lipolysis and Circumference Reduction of Abdomen When Compared to a Sham Treatment

Status Active, not recruiting

Clinical Trial Summary

The study is a prospective single-blinded two-arms study that includes three treatment procedures and four follow-up visits

Clinical Trial Description

This study will evaluate the clinical efficacy and safety of the BTL-899 device for non-invasive lipolysis and circumference reduction of abdomen. The study is a prospective single-blinded two-arms study. The subjects will be enrolled and assigned into a two study groups. All subjects will complete three (3) treatment visits and will be invited to four (4) follow-up visits 1, 2, 3 and 6-months after the final treatment. 6-months follow-up visit is the optional one. ;

Related Conditions & MeSH terms

• Improvement of Abdomen Appearance

• NCT number: NCT04000945
• Study type: Interventional
• Source: BTL Industries Ltd.
• Status: Active, not recruiting
• Phase: N/A
• Start date: December 3, 2018
• Completion date: December 31, 2019