FDA approved device for facial skin tightening

Trial ID:
IRB-22-7948
E. Victor Ross, M.D.
This study will evaluate the safety and effectiveness of the FDA approved UltraClear laser device for the improvement of skin appearance and skin texture. The cosmetic device uses a skin peeling process to improve skin properties such as softness, elasticity, and appearance. Participation in this study requires attending 5-6 study visits over a 7–8-month period. Study visits will take place at the Scripps Clinic Carmel Valley.
- Be between 18 and 75 years of age<br>- Have clinically identifiable photodamage on facial skin, neck, or chest<br>- Be willing and able to comply with all follow-up requirements<br>- Meet all other eligibility requirements

Contact Info:

  • Clinical Research Services
  • CRSLeadership@scrippshealth.org