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RECRUITING
NCT03334292

Natural History of Wilson Disease

Sponsor: Yale University

View on ClinicalTrials.gov

Summary

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.

Official title: Natural History of Wilson Disease: Registry for Patients With Wilson Disease

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

300

Start Date

2017-12-18

Completion Date

2029-11-15

Last Updated

2025-05-22

Healthy Volunteers

No

Conditions

Locations (6)

Yale University

New Haven, Connecticut, United States

Advent Health

Orlando, Florida, United States

Baylor College of Medicine

Houston, Texas, United States

Seattle Children's Hospital

Seattle, Washington, United States

Universitätsklinikum Heidelberg

Heidelberg, Germany

Royal Surrey Country Hospital

Guildford, Surrey, United Kingdom