The Efficacy Of The Wavelight Mydon Laser for Hair Removal And Treatment of Leg Veins
Completed · Not applicable
Conditions studied: Leg Veins, Hair Removal
In brief
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.
Key facts
- Study ID
- NCT00366964
- Run by
- University of California, Davis
- People needed
- 10
- Starts
- 2004-10-01
- Expected to finish
- 2006-04-01
- Last updated by the study team
- 2015-04-07
Who can join
Age: 18 and older. Sex: female. Healthy volunteers: accepted.
You may qualify if…
- Female patients of Asian and darker skin type greater than or equal to 18 years of age.
- Ability to give informed consent.
You may not qualify if…
- Pregnancy.
- Taking medications that are photosensitizing.
- History of skin disease in the area to be treated over the last 6 months.
- Ongoing cutaneous lupus erythematosus, morphea, alopecia areata, or severe folliculitis.
- History of keloidal or hypertrophic scarring.
- Have inadequate hair growth in the test area of axilla.
- Have unrealistic expectations of the treatment.
- Co-existing severe emotional, medical or surgical illness leading to the inability to meet the follow-up requirements.
Where it is running
- University of California, Davis Medical Center Department of Dermatology — Sacramento, California, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.