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Clinical Trial Summary

To evaluate the efficacy of Rapamycin in extended cervicofacial lymphatic malformations in pediatric patients. Rapamycin is administered oral for a 6 month period. The success rate is determined by volume reduction superior to 1/5e of the initial volume measured by MRI, impact on QOL and reduction of bleeding in case of mucosal involvement.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03243019
Study type Interventional
Source University Hospital, Lille
Contact Pierre Fayoux, MD
Phone 3 20 44 50 67
Email pierre.fayoux@chru-lille.fr
Status Recruiting
Phase Phase 2
Start date June 25, 2018
Completion date February 2025

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