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Clinical Trial Summary

To demonstrate the safety and performance of the Tixel fractional system for treatment of photodamage using low-energy settings.


Clinical Trial Description

A Prospective, single-center, single-arm clinical study of subjects who are seeking a procedure to reduce the appearance of photodamage, and meet study eligibility criteria, and have provided informed consent will be enrolled in the study. One investigational center will participate in the recruitment. Each study subject will receive 3 treatments with Tixel at 4-6 week intervals. Final follow-up will occur 3 months following the last treatment ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05182502
Study type Interventional
Source Main Line Center for Laser Surgery
Contact
Status Active, not recruiting
Phase N/A
Start date January 7, 2022
Completion date December 2023

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