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Study identifier: NCT01885767 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Neurofibromatosis (NF) Registry Portal

Condition: Neurofibromatosis 1 · Neurofibromatosis 2 · Schwannomatosis  ·  Sponsor: The Children's Tumor Foundation

PhaseN/A
Planned participants20000
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

The NF Registry is a database of patient-reported symptoms, treatments, and experiences with their neurofibromatosis disease. It is a contact registry to relay clinical trial opportunities to targeted patient subgroups, and to supply de-identified disease data to researchers. It has the potential to become a natural history resource.

This description comes directly from the study's public registry record.

Talk to the study team

Kate Kelts, B.S.N.  ·  646-738-8567  ·  kkelts@ctf.org

Annette Bakker, Ph.D.  ·  212-344-7029  ·  abakker@ctf.org

Always discuss trial participation with your own doctor first.

Locations (1)

Children's Tumor FundationNew York, New York, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT01885767