A Clinical Study to Evaluate the Efficacy and Satisfaction of Ultrasound Therapy Combined With SkinCeuticals A.G.E for Improving Facial Aging

Yes Skin Medical Group50 enrolled

Overview

A Prospective, Single-center, Single-blind, Randomized split-face, controlled trial will be conducted. The goal of this clinical trial is to evaluate the efficacy and satisfaction of ultrasound therapy combined with SkinCeuticals A.G.E in improving facial aging, and to explore the medical value of ultrasound therapy combined with SkinCeuticals A.G.E. Participants will be treated with ultrasound combined with SkinCeuticals A.G.E on one randomized side face and ultrasound combined with standard cream on the other side.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

Conditions

Skin Aging

Interventions

SkinCeuticals A.G.E

Eligibility

Sex: ALLMin age: 18 YearsMax age: 65 YearsHealthy volunteers:

Medical Language ↔ Plain English

Inclusion Criteria: 1. Chinese subjects aged 18-65 years inclusive; 2. The subject 's facial skin is rough, flaccid, and lack of elasticity; 3. Subjects with multiple facial fine lines (perioral/periocular/forehead, etc.), decree lines or puppet lines area with static fine lines trend, the lower part showed signs of loosening; 4. Subjects who have consistent facial skin status on both sides and plan to receive ultrasound therapy; 5. Subjects are willing to follow the requirements of the study protocol and complete the corresponding procedures; 6. Subjects understand the nature of the study and sign the informed consent form (ICF). Exclusion Criteria: 1. Subjects with contraindications to ultrasound treatment (such as malignant tumor, acute systemic infection, severe heart disease, bleeding tendency, etc.) or contraindications to A.G.E use (or allergic to other skin care components); 2. Subjects with facial skin diseases, infection, inflammation or allergic constitution that may affect the judgment of the test results; 3. Subjects with hypertrophic scar or scar constitution; 4. Receiving treatment of tightening medical treatment program (Thermage/Fotona 4D/ultrasound/microneedle, etc.) or planning to receive other tightening medical treatment program and drugs during this treatment in the past 3 months; 5. Patients who have oral or topical cosmetic products that may affect the test results within the past 2 weeks; 6. Subjects who have participated in drug clinical trials or other trials within the past 30 days (or are participating in), or have used drugs affecting the test results within 1 week; 7. Female subjects who are pregnant, lactating or plan to become pregnant; 8. Other subjects who are not suitable for participating in this study as assessed by the investigator.

Outcomes

Primary Outcomes

Global aesthetic improvement scale （GAIS） score

Investigator Satisfaction Assessment Form. Scoring criteria: 5 (very much improved), 4 (marked improvement), 3 (improved), 2 (no change), or 1 (worse).

Time frame: at day 90 after procedure

Secondary Outcomes

Change from baseline in fine lines score

Skin Parameter Assessment Form. Fine lines: Grading was performed on a Griffith 's scale (10-point scale) with different scores representing: 0 (no fine lines/wrinkles, skin completely smooth and no wrinkles); 1-3 (mild, few fine lines and wrinkles, and distant intervals within the treatment area); 4-6 (moderate, moderate number of fine lines/wrinkles within the treatment area and close to each other); and 7-9 (severe, dense clusters of fine lines/wrinkles within the treatment area). Fine lines status should be evaluated by an independent investigator.