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Natural History of Wilson Disease
RecruitingObservational study
Natural History of Wilson Disease: Registry for Patients With Wilson Disease
Who can join
All ages · All sexes
Full eligibility criteria
Inclusion Criteria: * 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) Exclusion Criteria: * Diagnosis of WD has been excluded * Unwilling to provide informed consent or assent
About the 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 · Participants: 300 · Started: Dec 18, 2017
Contact the study team
- Ricarda Tomlin · Phone: (203) 785-2073
- Sefa Keserci, PhD · Phone: (203) 3766043
Official record on ClinicalTrials.gov — NCT03334292
Locations in the U.S.
| Connecticut | Yale University, New Haven |
| Florida | Advent Health, Orlando |
| Texas | Baylor College of Medicine, Houston |
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.