Comparison of Efficacy, Safety and Tolerability of Two Different 810 nm Diode Lasers for Hair Red… (NCT01212172) | Clinical Trial Compass
CompletedPhase 3
Comparison of Efficacy, Safety and Tolerability of Two Different 810 nm Diode Lasers for Hair Reduction
United States20 participantsStarted 2010-09
Plain-language summary
The purpose of this research study is to compare two different 810 diode laser systems (Soprano XL (SHR Mode)and Light Sheer Duet) for laser hair removal. The goal is to determine if each laser system is effective at reducing the amount of hair on the lower legs or the axilla (arm pit). Another goal is determine the subject's perspective on the treatment including tolerability and effectiveness.
Who can participate
Age range18 Years
SexALL
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Inclusion criteria
✓. Subjects must be at least 18 years of age.
✓. Subjects must be in reasonably good health as defined by the Investigator.
✓. Subject agrees to avoid tanning during their participation in this trial.
✓. Subject has Fitzpatrick skin types I-V and dark brown hair.
✓. Subjects must agree to avoid shaving legs less than 72 hours prior to a study visit.
✓. Subjects have indicated willingness to participate in the study by signing an informed consent document.
Exclusion criteria
✕. Subject is pregnant, lactating, or planning to get pregnant within the study period.
✕. Subject is unwilling to use birth control during the study period if of child bearing age.
✕. Subject has a known history of photosensitivity or use of medication with photosensitizing properties.
✕. Subject has skin disease on exam at screening.
✕. Subject has history or evidence of any chronic or reoccurring skin disease or disorder(e.g., psoriasis, Netherton syndrome, etc.) affecting the treatment area.
✕. Subject has a history of keloid or hypertrophic scar formation.