An Evaluation of the Erchonia Laser As a Non-Invasive Treatment to Improve the Appearance of Skin Laxity
NCT06941610 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 35
Last updated 2025-09-11
Summary
The purpose of this clinical study is to determine the effectiveness of the Erchonia® GVS in improving the appearance of skin laxity on the abdominal region.
Conditions
- Skin Laxity
Interventions
- DEVICE
-
Erchonia GVS Laser
405nm violet and 520nm green laser light therapy.
Sponsors & Collaborators
-
Erchonia Corporation
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 22 Years
- Max Age
- 70 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-05-30
- Primary Completion
- 2026-08-01
- Completion
- 2026-11-01
- FDA Device
- Yes
Countries
- United States
Study Locations
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