N/A
N=9
Evaluation of Non-Ablative Laser for Treatment of Direct Brow Lift Scars
Scar
Bottom Line
View on ClinicalTrials.gov: NCT02032641 ↗Enrolled (actual)
9
Serious AEs
0.0%
Results posted
Jan 2017
Primary outcome: Primary: Relative Improvement — 50.0; 50.0 percentage of times treated scar chosen
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Laser treatment (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- University of Miami
- Primary completion
- May 2015
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Relative Improvement |
50.0; 50.0 | — |
| SECONDARY Overall Appearance |
3.75; 4.37; 6.25; 4.50 | <0.05 sig |
| SECONDARY Hair Loss |
1; 1 | — |
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.
Eligibility Criteria
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
Data sourced from ClinicalTrials.gov (NCT02032641). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.