Actively Recruiting
AdvaTx Laser Treatment for Vascular Birthmarks
Led by Szeged University · Updated on 2026-02-06
20
Participants Needed
1
Research Sites
55 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The primary objective of the present study is to get experiences with the use of CE-marked ADVATx laser treatment for port-wine stains. Secondary objectives: To investigate the clinical efficacy of ADVATx laser treatment for port-wine stains. To investigate the potential side effects (erythema, hyperpigmentation, oedema, pain, swelling, skin burning, blisters) of the treatment. Patients in the study will receive ADVATx laser treatment (1 treatment per month for 4 months) The treatment takes approximately 10-30 minutes per session. The treatment lasts for a total of 5 months for one patient. At each treatment session photographic documentation will be performed. PRO will be assessed by a questionnaire. At the end of the study, the patient rates the treatment and improvement on a Patient Satisfaction Scale.
CONDITIONS
Official Title
AdvaTx Laser Treatment for Vascular Birthmarks
Who Can Participate
Eligibility Criteria
You may qualify if you...
- The patient understands the study information, gives informed consent, and is able to participate
- Signed consent form is provided
- Parental consent is required for patients under 18 years old
- The treated lesions are at least 15 cm² in size
- Participants have Fitzpatrick skin types I to IV
You will not qualify if you...
- Lack of parental consent for patients under 18 years old
- Lesions located in the central part of the face (cheeks, nose)
- Participants with Fitzpatrick skin types V or VI
- Pregnancy
- Epilepsy
- Fever or infectious diseases
- Participation in another clinical trial within the past month or currently enrolled in one
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
University of Szeged, Albert Szent-Györgyi Clinical Centre, Department of Dermatology and Allergology
Szeged, Csongrád-Csanád Vármegye, Hungary, 6720
Actively Recruiting
Research Team
L
Lajos Kemény, professor, MD, DSc, MHAS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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