Ultrasound Device for Hair Removal
Status
Conditions
Treatments
Details and patient eligibility
About
The purpose of this study is to evaluate the safety and efficacy of the Cutera UHAIR ultrasound device for hair removal.
Full description
The purpose of this study is to evaluate the Cutera UHAIR device for safety and efficacy for removal and long term reduction of unwanted hair on subjects with Fitzpatrick skin types I-IV and dark (black or brown), red, and blonde colored hair.
At investigator's discretion, each subject will receive treatments and will be scheduled for follow-up visits after the final treatment. The treated area(s) will be photographed at each visit for analysis.
Enrollment
Sex
Ages
Volunteers
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
Trial design
Primary purpose
Allocation
Interventional model
Masking
10 participants in 1 patient group
Trial contacts and locations
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Data sourced from clinicaltrials.gov
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