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Clinical Study to Evaluate the Safety and Effectiveness of the Treatment With Tixel C on Acne Scars

Scars Clinical Trial

Official title:
A Prospective Study With Blinded Assessment to Evaluate the Safety and Effectiveness of the Tixel C Fractional System in the Treatment of Acne Scars

Clinical Trial Summary

The purpose of this research is to evaluate the safety and effectiveness of the Tixel C device for the treatment of acne scars, for improvement in the appearance of surface texture.

Clinical Trial Description

44 participents between two research locations with moderate acne scars will receive 3-5 treatments sessions with the Tixel C device according to investigator's review of subject response. Improvement of acne scarring will ve evaluated at 1 month, 3 months and 6 months post treatment. Post-treatment response will be evaluated as well as any incidence of side efects throughout the study. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04269317
Study type Interventional
Source Novoxel Ltd.
Contact
Status Withdrawn
Phase N/A
Start date March 1, 2020
Completion date January 10, 2021
View Details
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