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Circadian Variation of Urinary Copper Excretion in Wilson Disease Patients

Circadian Variation of Urinary Copper Excretion in Wilson Disease Patients Treated With Chelators or Zinc Salts

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06430359
Acronym
VARCUWIC
Enrollment
30
Registered
2024-05-28
Start date
2025-01-10
Completion date
2027-02-10
Last updated
2026-01-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Wilson Disease

Keywords

Wilson disease, urinary copper, chelator

Brief summary

Wilson's disease (WD) is a genetic disorder characterized by an accumulation of copper in the body, mainly in the liver and brain. Patients suffering from this disease are monitored by liver function tests, blood copper levels, and 24-hour urinary copper determinations. Treatment is based either on chelating the copper accumulated in the body using D-penicillamine or Trientine or on limiting intestinal copper absorption with zinc salts. Monitoring copper elimination in urine collected over 24 hours is essential for estimating a patient's copper load, adapting treatment dosage, and detecting any copper deficiency. Nevertheless, urine collection is often complicated for patients, given the obvious constraints of collecting urine over 24 hours. Without this, clinical decisions are usually made based on spot urine. There is no official recommendation for monitoring urinary copper elimination other than on 24-hour urine. According to studies on healthy volunteers under physiological conditions, urinary copper elimination occurs according to a circadian rhythm, with minimal copper elimination between 8 pm and 4 am and maximum between 8 am and noon. The study would aim to find the period of the day best correlated with 24h urinary copper excretion

Interventions

DIAGNOSTIC_TESTurine and blood test

3 urine collections of an 8h period. One blood sample for liver function test and copper assessment

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
6 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Patients with a confirmed diagnosis of Wilson's Disease (Leipzig score ˃4). * Age ≥ 6 years and ≤70 years. * Patient able to perform 24h urine. * Current treatment with D-Pencillamine, Trientine or Zinc. * Non-opposition of patient and/or legal representatives for minor patients.

Exclusion criteria

* Patients who had a change in treatment within the last 6 months before the inclusion * Patients who have undergone liver transplantation * Patients with known chronic renal failure (GFR \< 30 ml/min) * Patients on long-term diuretic or corticosteroid therapy * Persons deprived of liberty by a judicial or administrative decision * Patient under judicial protection, unable to express consent

Design outcomes

Primary

MeasureTime frameDescription
Correlation factorTwo 24-hour urine recollectionCorrelation between 24-hour urinary copper excretion and 8-hour urinary copper excretion collected between midnight and 8 am).

Countries

France

Contacts

Primary ContactEduardo COUCHONNAL, Dr
eduardo.couchonnal-bedoya@chu-lyon.fr04 27 35 70 50
Backup ContactAbdelouahed BELMALIH, PhD
abdelouahed.belmalih@chu-lyon.fr04 27 85 62 67

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026