← Eichor
Study identifier: NCT02995538 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Neurogenetics Patient Registry

Condition: Neurogenetic Disorders  ·  Sponsor: University of Pittsburgh

PhaseN/A
Planned participants1000
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

The objective of this project is to develop a Neurogenetics patient database and bio repository - which includes clinical information regarding history, physical examination, laboratory testing including genetic testing (NextGen sequencing including whole exome and whole genome sequencing, SNParray, etc.), neuroradiology studies, neurophysiology studies - all ordered as clinically deemed appropriate, natural history from clinical longitudinal follow-up and to use de-identified information from this registry/ repository, when appropriate for clinical and translational research.

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

Talk to the study team

Jennifer Baker, MA  ·  412-69-26378  ·  jennifer.baker@chp.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Children's Hospital of Pittsburgh of UPMCPittsburgh, Pennsylvania, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT02995538