Actively Recruiting
RFMN in Combination With 1927 nm Thulium Laser for Treating Photoaged Skin
Led by Universitätsklinikum Hamburg-Eppendorf · Updated on 2024-05-21
35
Participants Needed
1
Research Sites
63 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The appearance of the aging skin is influenced by different factors including by the reduced elasticity and increased laxity of the skin, the decreasing volume as well as pigmentation disorders and dilated vascular markings. Currently, there are different methods available to treat the aging skin. Here, the combined treatment of radiofrequency micro needling (RFMN) and thulium laser has been commonly used in clinical practice. The aim of this clinical study is to investigate the efficacy, patient satisfaction, safety of RFMN and thulium laser treatment in patients with facial, age-related skin laxity, wrinkles, and pigmented lesions.
CONDITIONS
Official Title
RFMN in Combination With 1927 nm Thulium Laser for Treating Photoaged Skin
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Men and women aged 30 years or older
- Good general health with no relevant previous diseases
- Presence of facial wrinkles, dermatochalasis, or pigment spots suitable for RFMN and thulium laser treatment
- Ability to understand and willing to provide informed consent
- Willing and able to attend scheduled follow-up visits
You will not qualify if you...
- Younger than 30 years
- Pregnant or breastfeeding
- Excessive subcutaneous fat under the cheeks
- Significant scarring in the treatment area
- Open wounds or lesions in the treatment area
- Severe or cystic acne on the face
- Metallic implants in the face or neck region
- Mental illnesses such as psychoses or body perception disorders
- Use of isotretinoin, other retinoids, psychotropic drugs, coumarins, or heparins within the last 2 weeks
- Facial fillers less than 4 weeks before or during the study
- Resurfacing procedures (fractional, ablative, nonablative) less than 2 months before or during the study
- Cosmetic or surgical procedures less than 6 months before or during the study
- Tendency to develop excessive scarring
- Lack of informed consent
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University Medical Center Hamburg-Eppendorf
Hamburg, Germany, 20251
Actively Recruiting
Research Team
L
L Nguyen
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
NON_RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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