Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07250997

PALLAS Laser for Skin Diseases

Led by Szeged University · Updated on 2026-02-06

50

Participants Needed

1

Research Sites

55 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary objective of this study is to get clinical experiences with the PALLAS laser in the treatment of skin conditions that respond well to UV light (vitiligo, psoriasis, alopecia areata, atopic dermatitis). The secondary objective is to assess how user-friendly is the Pallas laser in the treatment of skin diseases. The patient in the trial will receive UVB laser treatment (2 treatments per week for up to 3 months). The treatments will be carried out by the doctors participating in the trial. The treatment takes approximately 10 minutes per session, and can last up to 3 months per patient. Photographic documentation of the lesions to be treated and the lesions treated is taken at the start of the examination and then once a month. At the end of the study, the patient rates the treatment and improvement on a Patient Satisfaction Scale.

CONDITIONS

Official Title

PALLAS Laser for Skin Diseases

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Understands the study information and gives informed consent to participate
  • Has a skin condition expected to respond well to targeted UVB treatment
  • Signed consent form obtained
Not Eligible

You will not qualify if you...

  • Under 18 years of age
  • Pregnant
  • Has epilepsy
  • Has fever or infectious diseases
  • Currently enrolled in another clinical trial or was enrolled within the past month

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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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

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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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