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Trials / Completed

CompletedNCT05954065

An Evaluation of the Effect of the Erchonia Laser for Non-invasive Reduction of Submental Fat

An Evaluation of the Effect of the Erchonia Corporation CFL Laser for Non-invasive Reduction of Submental Fat

Status
Completed
Phase
Study type
Interventional
Enrollment
31 (actual)
Sponsor
Erchonia Corporation · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The purpose of this clinical study is to determine the effectiveness of the Erchonia® CFL (manufactured by Erchonia Corporation (the Company), in providing noninvasive fat reduction in the submental area.

Detailed description

This clinical study is a prospective open-label design with post-study independent blinded outcome analysis to evaluate the efficacy of the Erchonia® CFL Laser in providing a noninvasive fat reduction in the submental area. Participants will receive 8 treatments over the course of 4 weeks.

Conditions

Interventions

TypeNameDescription
DEVICEErchonia CFL Laser405nm violet and 520nm green laser light therapy.

Timeline

Start date
2023-07-12
Primary completion
2024-05-31
Completion
2024-09-30
First posted
2023-07-20
Last updated
2025-08-29
Results posted
2025-08-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05954065. Inclusion in this directory is not an endorsement.

An Evaluation of the Effect of the Erchonia Laser for Non-invasive Reduction of Submental Fat (NCT05954065) · Clinical Trials Directory