Natural History of Wilson Disease

Recruiting now

Conditions studied: Wilson Disease

In brief

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.

Key facts

Study ID

NCT03334292

Run by

Yale University

People needed

300

Starts

2017-12-18

Expected to finish

2029-11-15

Last updated by the study team

2026-06-22

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

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 is running

• Yale University — New Haven, Connecticut, United States (enrolling)
• Advent Health — Orlando, Florida, United States (enrolling)
• Baylor College of Medicine — Houston, Texas, United States (enrolling)
• Universitätsklinikum Heidelberg — Heidelberg, Germany (enrolling)
• Seattle Children's Hospital — Seattle, Washington, United States
• Royal Surrey Country Hospital — Guildford, Surrey, United Kingdom

Full record on ClinicalTrials.gov

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