NCT03270150

Effect of the BTL-899 Therapy for Non-invasive Lipolysis and Circumference Reduction of Abdomen

Evaluation of Safety and Efficacy of the BTL-899 Device for Non-invasive Lipolysis and Circumference Reduction of Abdomen

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 40 (actual)
• Sponsor: BTL Industries Ltd. · Industry
• Sex: All
• Age: 22 Years
• Healthy volunteers: Accepted

Summary

The study is a prospective open-label single-arm study that includes three treatment procedures and four follow-up visits.

Detailed 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 open-label single-arm study. The subjects will be enrolled and assigned into a single study group. 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.

Conditions

• Improvement of Abdomen Appearance

Interventions

Type	Name	Description
DEVICE	BTL-899	BTL-899

Timeline

• Start date: 2017-09-01
• Primary completion: 2018-09-19
• Completion: 2018-10-03
• First posted: 2017-09-01
• Last updated: 2023-04-12

Locations

1 site across 1 country: Bulgaria