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Safety and Efficacy of the BTL-785F Device for Non-invasive Reduction of Submental Fat

NCT05831332 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 56

Last updated 2023-10-26

No results posted yet for this study

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 reduction of submental fat and skin laxity treatment.

Conditions

  • Skin Laxity

Interventions

DEVICE

BTL-785-7

Treatment with the BTL-785F device with the BTL-785-7 applicator for non-invasive reduction of submental fat.

Sponsors & Collaborators

  • BTL Industries Ltd.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-03-06
Primary Completion
2023-08-30
Completion
2023-10-25

Countries

  • Bulgaria

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05831332 on ClinicalTrials.gov