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Trial · NCT04706429

Registered outcomes13

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryLeft ventricular mass indexed to body surface area (LVMi)12 monthsChange in LVMi (g/m2), measured using CMR, from baseline to week 52.
SecondaryUrine copper excretion12 monthsCumulative urine copper excretion, measured using urinary copper, assessed from baseline to weeks 13, 26, 39 and 52.
SecondaryExercise capacity12 monthsChange in exercise capacity, measured using cardiopulmonary exercise testing (CPET), assessed from baseline to week 52.
SecondaryNumber of non-sinus supraventricular heart beats, presence and amount of atrial fibrillation, number of ventricular-origin beats and presence and amount of non-sustained ventricular tachycardia12 months
Change in number of non-sinus supraventricular heart beats, presence and amount of atrial fibrillation, number of ventricular-origin beats and presence and amount of non-sustained ventricular tachycardia, in 24 hours, measured using ambulatory heart monitoring, assessed from baseline to week 52.
SecondaryCirculating high sensitivity troponin12 monthsChange in circulating high sensitivity troponin, assessed from baseline to week 52.
SecondaryLV global longitudinal strain, wall thickness, mass, volumes and ejection fraction (EF)12 monthsChange in LV global longitudinal strain, wall thickness, mass, volumes and ejection fraction (EF) measured using CMR, assessed from baseline to week 52.
SecondaryPeak left ventricular outflow12 monthsChange in peak left ventricular outflow tract gradient, measured using CMR, assessed from baseline to week 52.
SecondaryAtrial volume and function12 monthsChange in atrial volume and function, measured using CMR, assessed from baseline to week 52.
OtherLV myocardial cellular mass12 monthsChange in LV myocardial cellular mass, measured using CMR, from baseline to week 52.
OtherLV myocardial extracellular mass12 monthsChange in LV myocardial extracellular mass, measured using CMR, from baseline to week 52.
OtherLV myocardial extracellular volume12 monthsChange in LV myocardial extracellular volume, measured using CMR, from baseline to week 52.
OtherLV late gadolinium enhancement12 monthsChange in LV late gadolinium enhancement, measured using CMR, from baseline to week 52.
OtherPCr/ATP ratio12 monthsChange in PCr/ATP ratio, measured using 31P MRS (sub-group), from baseline to week 52.

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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