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Study identifier: NCT03920774 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

The Natural History of Familial Dysautonomia

Condition: Familial Dysautonomia (Riley-Day Syndrome) · Hereditary Sensory and Autonomic Neuropathies · Hereditary Sensory and Autonomic Neuropathy 3  ·  Sponsor: NYU Langone Health

PhaseN/A
Planned participants400
Who can joinAll sexes, 4 Years to no upper limit
Healthy volunteersNo

About this study

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.

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

Talk to the study team

Britney A. Paredes Lopez  ·  2122637225  ·  Britney.ParedesLopez@nyulangone.org

Horacio Kaufmann, MD  ·  horacio.kaufmann@nyulangone.org

Always discuss trial participation with your own doctor first.

Locations (2)

Dysautonomia Center - School of Medicine -NYU Langone Medical CenterNew York, New York, United StatesRecruiting
Sheba Medical Center - Safra Children's HospitalTel Litwinsky, Ramat Gan, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT03920774