Ultrasound Device for Hair Removal (NCT01057134) | Clinical Trial Compass
CompletedNot Applicable
Ultrasound Device for Hair Removal
10 participantsStarted 2010-03
Plain-language summary
The purpose of this study is to evaluate the safety and efficacy of the Cutera UHAIR ultrasound device for hair removal.
Who can participate
Age range18 Years – 90 Years
SexALL
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Inclusion Criteria:
* Male or female at least 18 years of age
* Fitxpatrick skin type I-IV
* Area with unwanted hair
* Subject must be able to read, understand and sign the consent form
* Subject must adhere to the follow-up schedule and study instruction
Exclusion Criteria:
* Simultaneous participation in any other clinical study
* Inability or unwillingness to follow the treatment schedule
* Inability or unwillingness to sign the informed consent
* Infection in the target area
* Any disease or condition that could impair wound healing
* History of keloid formation
* History of malignant tumors in the target area
* Skin abnormalities in the target area, e.g. cuts, scrapes, wounds, scars, large moles
* History of hair removal in target area (light based or electrolysis)
* Pregnant or lactating
What they're measuring
1
Reduction in Hair Count in the Treated Area
Timeframe: baseline and 3 months post final treatment (up to 28 weeks)