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A Registered Cohort Study on Wilson's Disease

W

Wan-Jin Chen

Status

Enrolling

Conditions

Wilson's Disease

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT04012658
MRCTA,ECFAH OF FMU[2019]197

Details and patient eligibility

About

The aim of this study is to determine the clinical spectrum and natural progression of Wilson's Disease in a prospective multicenter natural history study, to assess the clinical, genetic, epigenetic features and biomarkers of patients with Wilson's Disease to optimize clinical management.

Enrollment

2,000 estimated patients

Sex

All

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients with the genetic diagnosis of Wilson's Disease
  • Asymptomatic Wilson's Disease carriers
  • Relatives of Wilson's Disease patients or carriers
  • Unrelated healthy controls
  • Participants or Parent(s)/legal guardian(s) willing and able to complete the informed consent process

Exclusion criteria

* Participants are unable to comply with study procedures and visit schedule

Trial design

2,000 participants in 4 patient groups

Patients with the genetic diagnosis of Wilson's Disease
Treatment:
Other: No intervention
Asymptomatic Wilson's Disease carriers
Treatment:
Other: No intervention
Relatives of Wilson's Disease patients or carriers
Treatment:
Other: No intervention
Unrelated healthy controls
Treatment:
Other: No intervention

Trial contacts and locations

1

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Central trial contact

Jin He, MD; Yi Lin, MD.PhD

Data sourced from clinicaltrials.gov

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