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Clinical Trial Summary

This study will evaluate the tolerability and effectiveness of four FDA-approved treatments in Neurofibromatosis Type 1 Cutaneous Neurofibromas. These treatments are: a 1064nm laser, a 755nm laser, and Kybella and Polidocanol injections. Each patient will have a treatment and a control site. This study is designed with the goal of improved efficacy/tumor reduction via multiple treatment visits. If there is minimal to no clinical improvement in tumor size with one treatment after three treatment visits, the subject will be given the option of crossover treatment with the most effective of the four treatments. Three treatment visits with the crossover treatment will then take place.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06300502
Study type Interventional
Source Massachusetts General Hospital
Contact Devon Gunter
Phone 617-724-2168
Email wellmancrc@partners.org
Status Not yet recruiting
Phase Phase 1
Start date June 2024
Completion date December 2025

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