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Performance of PicoWayTM Picosecond Fractional Laser for Acne Scars

Acne Scars - Mixed Atrophic and Hypertrophic Clinical Trial

Official title:
Clinical Study to Evaluate the Performance of the PicoWayTM Picosecond Fractional Laser for Treatment of Acne Scars

Clinical Trial Summary

Open-label, prospective study. Up to 60 healthy adult volunteers seeking facial acne scars treatment, males or females of 18 to 75 years of age, from up to 3 investigational sites.

Clinical Trial Description

Subjects in this study will receive up to six (6) treatments in 3-8 weeks interval, with the PicoWayTM device-fractional handpiece 532nm and/or 1064nm according to the study protocol. Subjects will be followed by phone 7 days post first treatment by study staff, and will return for two follow‐up (FU) visits at the clinic at: 6 weeks and 12 weeks following the last treatment.

Methodology described in the protocol to evaluate efficacy and safety of treatments will be carried out at each visit at the clinic. ;

Study Design

Related Conditions & MeSH terms

  • Acne Scars - Mixed Atrophic and Hypertrophic
  • Hypertrophy
Clinical Trial Details
NCT number NCT02592993
Study type Interventional
Source Syneron Medical
Contact
Status Active, not recruiting
Phase N/A
Start date May 23, 2015
Completion date August 2017
View Details
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