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
| Type | Name | Description |
|---|---|---|
| DEVICE | Laser Treatment | The 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. |
| DEVICE | Wave Light laser device for skin treatment | To 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.