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Spanish Wilson Disease Registry

NCT06466291 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 600

Last updated 2024-06-20

No results posted yet for this study

Summary

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.

Conditions

  • Wilson Disease

Sponsors & Collaborators

  • Asociación Española para el Estudio del Hígado

    lead OTHER

Principal Investigators

  • Zoe Mariño · Asociación Española para el Estudio del Hígado

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-12-02
Primary Completion
2030-12-31
Completion
2030-12-31

Countries

  • Spain

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06466291 on ClinicalTrials.gov