To evaluate the safety and effectiveness of the Excel V system for the treatment of lower extremity spider veins on the ankles.
The purpose of this study is to evaluate the real-world effectiveness of the 532 nm and 1064 nm Nd:YAG lasers within the Cutera Excel V system for the treatment of lower extremity spider veins, specifically on the ankles, within a clinic setting.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
4
Treatment of lower extremity spider veins
DuPage Medical Group
Naperville, Illinois, United States
Physician Global Assessment of Improvement in Treated Spider Veins on the Ankles
Improvement in treated ankle spider veins at 4 weeks post final laser treatment (compared to baseline) as assessed by a blinded evaluators Physician Global Assessment Scale score (Min=0; 4= Max). Higher Score Indicates Better Outcome.
Time frame: Four weeks post final laser treatment.
Subject Satisfaction With Improvement in Treated Spider Veins on the Ankles
Subject satisfaction with improvement in spider veins on the ankles as assessed using the Subject Satisfaction Assessment scale (Min=1, Max=5) at 4 weeks post final treatment. Higher score indicates better outcome.
Time frame: Four weeks post final laser treatment
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