RecruitingNCT03920774

The Natural History of Familial Dysautonomia

Natural History of Familial Dysautonomia


Sponsor

NYU Langone Health

Enrollment

400 participants

Start Date

Feb 22, 2017

Study Type

OBSERVATIONAL

Conditions

Summary

The study will collect clinical information from patients with FD and allow them to give blood to help develop biological markers of the disease to aid diagnosis and treatment. This is a non-invasive, non-interventional, observation study that poses only minimal risk for participants. The study will document the clinical features of patients with FD overtime by storing their routine clinical test results in a central database. The study will involve collaborators at other specialist clinics around the world who follow/evaluate patients with FD annually. Providing blood for future use is optional.


Eligibility

Min Age: 4 Years

Inclusion Criteria2

  • Patients of any age with a diagnosis of familial dysautonomia (FD) with molecular confirmation of the IKBKAP mutation.
  • Ability to provide informed consent (or assent) and comply with the study protocol

Exclusion Criteria1

  • Subjects that do not wish to be a part of the study.

Interested in this trial?

Get notified about updates and connect with the research team.


Locations(2)

Dysautonomia Center - School of Medicine -NYU Langone Medical Center

New York, New York, United States

Sheba Medical Center - Safra Children's Hospital

Tel Litwinsky, Ramat Gan, Israel

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT03920774