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Safety and Efficacy Investigation on the Effects of ClearSkin Non-ablative ER:Glass 1540nm Laser Module in the Treatment of Acne Scars.

Acne Scars - Mixed Atrophic and Hypertrophic Clinical Trial

Official title:
Open-label, Safety, and Efficacy Investigation on the Effects of ClearSkin Non-ablative ER: Glass 1540nm Laser Module in the Treatment of Acne Scars.

Clinical Trial Summary

The ClearSkin module, Er: Glass 1540nm, is largely used in the treatment of acne vulgaris and acne scars. The non-ablative ER:Glass 1540 nm laser deeply penetrates the skin, causing thermal damage to the sebaceous glands, destroying P. acnes bacteria and reducing sebum production, while leaving the epidermis intact. The integrated vacuum mechanism extracts accumulated sebaceous material from the pores, while contact cooling protects the skin, reducing pain and allowing for safer and more effective treatment of the sebaceous glands within the dermis. Based on this background, the investigators have considered a pilot study aimed at assessing the efficacy and safety of the ClearSkin Module in treating subjects with facial acne scars.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Acne Scars - Mixed Atrophic and Hypertrophic
  • Hypertrophy
Clinical Trial Details
NCT number NCT06102343
Study type Interventional
Source Alma Lasers
Contact Natalie Dror, PhD
Phone +972528264282
Email natalie.dror@almalasers.co.il
Status Not yet recruiting
Phase N/A
Start date January 1, 2024
Completion date January 1, 2025
View Details
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