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

University of California (UC) Davis

Status: Completed

Conditions: Leg Veins; Hair Removal

Treatments: Device: Wave Light laser device for skin treatment; Device: Laser Treatment

Study type: Interventional

Funder types: Other

Identifiers

NCT00366964

200412776-1

Details and patient eligibility

About

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.

Full 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.

Enrollment: 10 patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

1. Female patients of Asian and darker skin type greater than or equal to 18 years of age.
2. Ability to give informed consent.

Exclusion criteria

1. Pregnancy.
2. Taking medications that are photosensitizing.
3. History of skin disease in the area to be treated over the last 6 months.
4. Ongoing cutaneous lupus erythematosus, morphea, alopecia areata, or severe folliculitis.
5. History of keloidal or hypertrophic scarring.
6. Have inadequate hair growth in the test area of axilla.
7. Have unrealistic expectations of the treatment.
8. Co-existing severe emotional, medical or surgical illness leading to the inability to meet the follow-up requirements.

Trial design

Primary purpose: Treatment

Allocation: Non-Randomized

Interventional model: Single Group Assignment

Masking: Single Blind

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10 participants in 1 patient group

Device

No Intervention group

Treatment:

Device: Wave Light laser device for skin treatment

Device: Laser Treatment