Aging Problems Clinical Trial
Official title:
Needless Laser Injector Versus Needle Injection for Antiaging Effect of Dermal Filler: A Randomized Split-face Comparison
Verified date | January 2023 |
Source | Seoul National University Bundang Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The investigators aimed to evaluate the efficacy and safety of needless laser injector for antiaging effect of dermal filler.
Status | Completed |
Enrollment | 24 |
Est. completion date | December 1, 2022 |
Est. primary completion date | August 31, 2022 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 25 Years to 60 Years |
Eligibility | Inclusion Criteria: - patients who wanted to improve facial skin aging Exclusion Criteria: - a history of skin rejuvenation treatment (including filler, botulinum toxin, lasers, chemical peeling, and topical retinoid) within 6 month prior to the start of the study - having a plan for skin rejuvenation treatment during the study - current pregnancy or breastfeeding - an allergy to polylactic acid (PLA) or hyaluronic acid (HA) - uncontrolled medical diseases |
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Seoul National University Bundang Hospital | Seongnam |
Lead Sponsor | Collaborator |
---|---|
Seoul National University Bundang Hospital |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Skin hydration using a Corneometer® CM 825 | at 12 weeks after treatment | ||
Secondary | Skin elasticity using a Cutometer® MPA 580 | at 12 weeks after treatment | ||
Secondary | Erythema index (EI) using a Mexameter® MX 18 (Courage & Khazaka) | at 12 weeks after treatment | ||
Secondary | Skin aging analyzed by three-dimensional photogrammetry | at 12 weeks after treatment | ||
Secondary | Patient's satisfaction score for antiaging effects | from 1 (extremely dissatisfied) to 7 (extremely satisfied) | at 12 weeks after treatment | |
Secondary | Patient's pain score during treatment | from 0 (none) to 10 (worst) | up to 24 weeks | |
Secondary | Adverse events related to the procedure | up to 24 weeks |
Status | Clinical Trial | Phase | |
---|---|---|---|
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