RecruitingWilson Disease
Natural History of Wilson Disease
Eligible age
All ages
Accepts
All genders
Locations
4 states
Healthy volunteers
No
See if you qualify for this study
Answer a few quick questions about your location and health. Takes about a minute.
About this study
The purpose of the registry/repository is to provide a mechanism to store data and specimens to support the conduct of future research about Wilson disease (WD). The overall aim is to determine the optimal testing for diagnosis and parameters for monitoring treatment of WD that will aid product utilization and development.
Sponsor: Yale University
You may qualify if…
- ✓ Known diagnosis of WD
- ✓ Able and willing to provide informed consent for adults (Parental/guardian permission (informed consent) and if appropriate, child assent for participants \<18 (or per local Institutional Review Board (IRB) regulation)
You may not qualify if…
- ✕ Diagnosis of WD has been excluded
- ✕ Unwilling to provide informed consent or assent
Where it's recruiting
Source: ClinicalTrials.gov · NCT03334292 · last updated 2026-06-22