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Clinical Trial Summary

This is an open-label, single-center study. Subjects in this study will receive up to four (4) facial treatments at 4-6 (±1) weeks interval, with the VBeam Prima device according to the study protocol. Subjects will return for follow‐up (FU) visits at the clinic at 1 and 3 months following the last treatment.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03383705
Study type Interventional
Source Syneron Medical
Contact Gilly Munavalli, MD
Phone (704) 375-6766
Email info@carolinaskin.com
Status Recruiting
Phase N/A
Start date November 15, 2017
Completion date November 15, 2018