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About
A general protocol to treat a variety of dermatologic conditions and collect patient feedback.
Primary outcome is the collection and analysis of patient questionnaires related to the overall experience of the device treatment. Secondary outcome measures include physician and subject evaluations in regards to improvement seen in the device as well as assessment of side effects.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Male or female subjects between 18 to 70 years of age.
Dermatologic condition that can be addressed by the laser, including but not limited to:
Willingness to have digital photographs taken of treatment area(s) and agreement with use of photographs for presentation, educational, or marketing purposes.
Willingness to comply with the following during the study, including the follow-up period:
Willingness and ability to comply with study instructions and return for required visits.
Subject has read and signed a written informed consent form.
Subject lives within 50 miles of study site.
Willingness to shave hair in intended treatment area
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
200 participants in 1 patient group
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Central trial contact
Alexander Denis
Data sourced from clinicaltrials.gov
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