RecruitingNCT01885767

Neurofibromatosis (NF) Registry Portal

Neurofibromatosis (NF) Registry Portal Funded by Children's Tumor Foundation


Sponsor

The Children's Tumor Foundation

Enrollment

20,000 participants

Start Date

Jun 1, 2012

Study Type

OBSERVATIONAL

Conditions

Summary

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.


Eligibility

Inclusion Criteria3

  • Diagnosed with NF1
  • Diagnosed with NF2
  • Diagnosed with Schwannomatosis

Exclusion Criteria1

  • Failure to complete account registration

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Locations(1)

Children's Tumor Fundation

New York, New York, United States

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NCT01885767


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