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Spanish Wilson Disease Registry

A

Asociación Española para el Estudio del Hígado

Status

Enrolling

Conditions

Wilson Disease

Study type

Observational

Funder types

Other

Identifiers

NCT06466291
HCB/2021/1099

Details and patient eligibility

About

The main objective and purpose of the Registry is to know the current status of Wilson Disease in Spain.

As secondary objectives, the prevalence and incidence of the disease will be analysed.

Likewise, the analysis aims to define future areas of interest in its pathogenesis, diagnosis, natural history, follow-up, prognosis and treatment.

Improving knowledge at a national level can help to design screening strategies and improve diagnostic circuits.

Full description

Retrospective and prospective study.

Enrollment

600 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with a confirmed Wilson Disease diagnosis

Exclusion criteria

  • Refusal to sign the informed consent for the study

Trial contacts and locations

1

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Central trial contact

Asociación Española para el Estudio del Hígado Asociación Española para el Estudio del Hígado

Data sourced from clinicaltrials.gov

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