About this trial
Wilson disease (WD) is a rare autosomal recessive disorder caused by a genetic defect in ATP7B resulting in limited excretion of excess copper into the bile Pathological copper accumulation occurs in the entire body, with the liver and the brain being primarily affected
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
All patients diagnosed with Wilson's
Disqualifiers
Claustrophobia
Refusal to share information
Heart failure
Trial population
All patients with Wilson's disease attending outpatient clinic
Trial design
Case-crossover
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
evaluate spectrum of cardiac affection by copper deposition in Wilson disease patients and detect early cardiac affection
Evaluate the effect of copper on EF and diastolic function of LV and RV
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: