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Nonablative Fractional Diode Laser for Treatment of Skin Resurfacing and Pigmented Lesions

Pigmented Lesions Clinical Trial

Official title:
Clinical Evaluation of a Nonablative Fractional 1940 nm Diode Laser for Skin Resurfacing and Treatment of Pigmented Lesions

Clinical Trial Summary

This study is intended to evaluate the efficacy and safety of a new diode fractional laser for skin resurfacing and treatment of pigmented lesions.

Clinical Trial Description

This study is a prospective, open-label, clinical trial to study the effects of the nonablative, fractional diode laser for skin resurfacing. Up to 60 eligible participants will be enrolled at up to three (3) sites. Participants will receive up to 4 treatments to the face, and other off-face locations may be treated. Participants will complete follow-up visits for clinical evaluation and photography at 1 and 3 months after the final treatment. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04203745
Study type Interventional
Source Candela Corporation
Contact
Status Completed
Phase N/A
Start date September 18, 2019
Completion date August 5, 2021
View Details
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