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Clinical Trial Summary

The goal of this study is to learn about treatment of port wine birthmarks treated with an FDA-approved 532 nm laser. The main questions it aims to answer are: - How well are the treatments tolerated? - Are there differences in tolerability of the treatment when a single high fluence laser pulse is used (the standard treatment) versus using multiple low fluence pulses? - Are there differences in results when using a single high fluence pulse versus multiple low fluence pulses? type of study: Clinical Trial Participants will undergo 3 monthly laser treatments with the 532 nm DermaV laser. Part of their birthmark will be treated with the standard single-pulse high fluence approach, and other parts will be treated with the multiple-pulse low fluence approach.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05841628
Study type Interventional
Source Massachusetts General Hospital
Contact Cemre Turk, MD
Phone 6175133337
Email cturk@mgh.harvard.edu
Status Recruiting
Phase N/A
Start date May 1, 2023
Completion date December 2024

See also
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Completed NCT03181984 - Postmarketing Safety Study of Hemoporfin in Patients With Port Wine Stain Phase 4
Completed NCT03125057 - A Pilot Study of Hemoporfin PDT in Children With Port-wine Stain Phase 4
Completed NCT02051101 - Pathogenic Mechanisms of Port Wine Stain and Repository of Port Wine Stain Biopsy Samples N/A