A Clinical Evaluation of the Treatment of Spider Veins on the Ankles

Not Applicable

Completed

Brief Summary: To evaluate the safety and effectiveness of the Excel V system for the treatment of lower extremity spider veins on the ankles.

Detailed Description: 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.

Recruitment & Eligibility

Inclusion Criteria

Males or females, 20 to 75 years of age (inclusive).
Fitzpatrick Skin Type I - III.
Having spider veins on at least 1 ankle measuring 2.0mm or less in diameter, linear or branching, and red, pink, blue and/or purple in color, as assessed by the investigator.
Having spider veins on the ankle that are appropriate for laser treatment, as assessed by the investigator.
Subject must be able to read, understand and sign the Informed Consent Form.
Subject must be willing and able to adhere to the treatment and follow-up schedule and post-treatment care instructions.
Wiling to have limited sun exposure for the duration of the study, including the follow-up period.
Willingness to have digital photographs taken of ankle spider veins and agree to use of photographs for presentation, educational or marketing purposes.
Agree not to undergo any other procedure for the treatment of ankle spider veins during the study.

Exclusion Criteria

Fitzpatrick Skin Type IV - VI.
Pregnant.
Having an infection, dermatitis or a rash in the treatment area.
Having significant varicosities or perforator veins.
History of pigmentary disorders, particularly tendency for hyper- or hypo-pigmentation.
Systemic use of isotretinoin (Accutane®) within 6 months of study participation.
Excessively tanned in areas to be treated or unable/unlikely to refrain from tanning during the study.
In the opinion of the investigator, any physical or mental condition which might make it unsafe for the subject to participate in this study or which requires systemic therapy that could interfere with this research study.

Primary Outcome Measures

Name	Time	Method
Physician Global Assessment of Improvement in Treated Spider Veins on the Ankles	Four weeks post final laser treatment.	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.

Secondary Outcome Measures

Name	Time	Method
Subject Satisfaction With Improvement in Treated Spider Veins on the Ankles	Four weeks post final laser treatment	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.