About this trial

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 criteria

Qualifiers

Diagnosed with NF1

Diagnosed with NF2

Diagnosed with Schwannomatosis

Disqualifiers

Failure to complete account registration

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

20,000 Participants
are grouped into 3 trial groups

Locations

1
Children's Tumor Fundation10017, New YorkNew York, United States

Sponsors and collaborators

The Children's Tumor Foundation

Lead sponsor