- Natural History of Wilson Disease — Recruiting • Gastroenterology • NCT03334292.
- What is being tested: A registry collecting clinical data and biological specimens from Wilson disease patients to establish optimal diagnostic testing methods and disease monitoring parameters, supporting future research into this rare genetic disorder of copper metabolism.
- Patient eligibility overview: The study enrolls individuals with confirmed or suspected Wilson disease across all age groups and disease stages, creating a comprehensive cohort for natural history characterisation and longitudinal follow-up.
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
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.
- : * 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
Use the source registry for the full inclusion and exclusion criteria before discussing referral or enrolment.