Clinical Trials Directory

Trials / Completed

CompletedNCT00366964

The Efficacy Of The Wavelight Mydon Laser for Hair Removal And Treatment of Leg Veins

Determine The Efficacy Of The Wavelight Mydon Laser For Hair Removal And Treatment of Leg Veins

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
10 (actual)
Sponsor
University of California, Davis · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

This study is being done to compare the efficacy of an FDA cleared laser device with other similar systems in the market for the treatment of leg veins and hair removal in patients with darker skin type.

Detailed description

The specific aim of the study is to determine the efficacy of this FDA approved laser for hair removal and treatment of leg veins in female patients having darker skin types (Fitzpatrick Skin type III-VI) and compare it with the efficacy of other similar commercial units available in the U.S.

Conditions

Interventions

TypeNameDescription
DEVICELaser TreatmentThe laser treatment involves the use of an FDA approved laser device (510K Clearance certificate) for hair removal and treatment of leg veins for females having skin types III - VI. The pulses are of appropriate energy and pulse duration based on the skin type.
DEVICEWave Light laser device for skin treatmentTo determine efficacy of FDA approved Laser treatment for hair removal and leg veins. The Mydon Wavelight is a Long Pulsed Nd Yag Laser, Class IV 1064 nm 55W

Timeline

Start date
2004-10-01
Primary completion
2006-04-01
Completion
2006-04-01
First posted
2006-08-22
Last updated
2015-04-07

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00366964. Inclusion in this directory is not an endorsement.