Actively Recruiting
Safety and Efficacy Assessment for the Temporary Facial Skin Tightening Improvement Effect Using the Monopolar Radiofrequency Device
Led by CLASSYS Inc. · Updated on 2026-03-13
96
Participants Needed
1
Research Sites
55 weeks
Total Duration
On this page
Sponsors
C
CLASSYS Inc.
Lead Sponsor
C
Chung-Ang University Hosptial, Chung-Ang University College of Medicine
Collaborating Sponsor
AI-Summary
What this Trial Is About
The purpose of this clinical trial is to demonstrate the temporary improvement in skin elasticity and to evaluate the safety of the investigational medical device that uses radiofrequency current when applied to the face (both cheeks), compared with the control device.
CONDITIONS
Official Title
Safety and Efficacy Assessment for the Temporary Facial Skin Tightening Improvement Effect Using the Monopolar Radiofrequency Device
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants aged 19 to under 65 years at the time of consent
- Average Cutometer R7 skin elasticity value for both cheeks of 0.6 or less
- Consent to photographic documentation for skin type and treatment evaluation
- Agreement to avoid other procedures or therapies that affect skin elasticity during the study
- Agreement to use medically acceptable contraception for up to 4 weeks after study completion
- Ability to understand study goals, provide written informed consent, and complete the study
You will not qualify if you...
- Presence of medical or skin conditions on the treatment area that could affect study conduct or results
- Presence of scars or open lesions on the treatment area
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Classys Inc
Seoul, South Korea, 06220
Actively Recruiting
Research Team
J
Jihye Min
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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