Clinical Trials Directory

Trials / Completed

CompletedNCT02146820

Picosecond Laser for Ttreatment of Benign Pigmented Lesions

LASER TREATMENT OF BENIGN PIGMENTED LESIONS WITH A DUAL WAVELENGTH PICOSECOND LASER

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Syneron Medical · Industry
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine whether Pico laser is effective and safe in the treatment of benign pigmented lesions.

Detailed description

The Investigational device is a dual wavelength laser system developed for treatment of pigmented lesions and for tattoo removal. The base unit is a GentleMax system modified to emit light at wavelengths of 532 and 1064 nm and deliver pulse energy up to 400mJ, and pulse duration of 700 ps.

Conditions

Interventions

TypeNameDescription
DEVICEGentleMax systemPicosecond Laser System for the Treatment of Pigmented Lesions

Timeline

Start date
2013-12-01
Primary completion
2015-05-01
First posted
2014-05-26
Last updated
2015-06-26

Locations

2 sites across 2 countries: United States, China

Source: ClinicalTrials.gov record NCT02146820. Inclusion in this directory is not an endorsement.