Abstract | BACKGROUND: OBJECTIVES: MATERIALS AND METHODS: An intraindividual randomized controlled trial (RCT) with split lesion design and single-blinded outcome evaluations. Patients received four NAFL treatments at monthly intervals. Primary endpoint was a blinded on-site visual and palpable Physician Global Assessment ( PhGA). Adverse event registration and pain evaluation were used to evaluate safety. Patient global assessment ( PGA) was a secondary endpoint to additionally evaluate efficacy. RESULTS: The PhGA did not find a statistically significant difference between the treated and untreated control side of 18 patients, although there was significant difference on the PGA 1 (p = .006) and 3 (p = .02) months after last treatment (Wilcoxon signed rank test). Patients experienced moderate pain during treatment and mild adverse events. CONCLUSION: In this trial, blinded PhGA could not confirm the clinical efficacy of 1540-nm nonablative fractional laser in the treatment of hypertrophic scars, but the treatment is safe, and patients judged that the treated part had a better global appearance.
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Authors | Evelien Verhaeghe, Katia Ongenae, Jessica Bostoen, Jo Lambert |
Journal | Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.]
(Dermatol Surg)
Vol. 39
Issue 3 Pt 1
Pg. 426-34
(Mar 2013)
ISSN: 1524-4725 [Electronic] United States |
PMID | 23279702
(Publication Type: Journal Article, Randomized Controlled Trial, Research Support, Non-U.S. Gov't)
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Copyright | © 2012 by the American Society for Dermatologic Surgery, Inc. Published by Wiley Periodicals, Inc. |
Topics |
- Adult
- Cicatrix, Hypertrophic
(surgery)
- Female
- Humans
- Laser Therapy
(adverse effects, methods)
- Male
- Middle Aged
- Prospective Studies
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