CompletedNot Applicable

Evaluation of Non-Ablative Laser for Treatment of Direct Brow Lift Scars

United States9 participantsStarted 2013-06

Plain-language summary

The purpose of this study is to determine the efficacy of the 1064nm Neodymium yttrium aluminum garnet (Nd:YAG) laser (Laser Genesis, Cutera TM) in the treatment of surgical scar after direct brow lift.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Undergoing or have undergone direct brow lift Exclusion Criteria: * under 18 years old * history of photodermatoses * receiving systemic isotretinoin within the preceding 6 months * undergoing other scar treatment in the brow area * pregnant patients * history of adverse outcomes related to non-ablative laser

What they're measuring

Relative Improvement

Timeframe: 1 month after final treatment

Trial details

NCT IDNCT02032641

SponsorUniversity of Miami

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-05

Results submitted2016-04-05

View on ClinicalTrials.gov More Scar trials