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NCT Number: NCT04965558

Clinical Features and Outcome in Patients With Osseomuscular Type of Wilson's Disease

The investigators aimed to observe the clinical features and outcome in patients with osseomuscular type of Wilson's disease from a large cohort during long-term follow-up

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Key information

Age range

6 year–65 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Second Affiliated Hospital, Zhejiang University School of Medicine

Hangzhou, Zhejiang, 310005, China

Location status: Recruiting

Location contact

Yi Dong

CONTACT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • genetically diagnosed WD patients

Exclusion criteria

  • Deny follow-up

Treatment and study plan

No intervention

Other

No intervention

Primary outcomes

  1. Serum ceruloplasmin

    Time frame: From 2004 through 2030

    Serum ceruloplasmin levels were collected among patients with wilson disease. After confirming a non-Gaussian distribution, the reference range of serum ceruloplasmin level was determined.

  2. Urinary Copper Excretion

    Time frame: From 2004 through 2030

    The measurement of 24-hour urine copper excretions were collected and measured.

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Second Affiliated Hospital, School of Medicine, Zhejiang University

Other

Registry information

Important dates

Study start
2004
Primary completion
2025
Study completion
2030
First posted
Jul 16, 2021
Registry last updated
Jul 16, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.