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Trial · NCT05014061

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryThe resolution of myocardial stunning at 48 hours (StunningRes48h).48 hours
The proportion of stunning that has resolved at 48 hours will be calculated according to the formula: StunningRes48h = (%AkinesiaBaseline - %Akinesia48h) / (%AkinesiaBaseline - %Akinesia30days) where %AkinesiaT is defined as the endocardial length of the akinetic myocardium measured in end-diastole divided by the total endocardial length measured in end-diastole in the 2- and 4-chamber view, at time T (T= 48h or 30 days)
SecondaryInfarct size6 monthsInfarct size, assessed by cardiac magnetic resonance imaging
SecondaryEjection fractionDay 1, Day 2, Day 3, Day 7, Day 14, Day 30 and 6 monthsEjection fraction, assessed by echocardiography
SecondarySustained ventricular tachycardia or fibrillation72 hoursAny sustained ventricular tachycardia or fibrillation within 72 hours
SecondaryHigh-grade atrioventricular block or sinus arrest72 hoursAny high-grade atrioventricular block or sinus arrest within 72 hours
SecondaryCardiac assist device72 hoursImplantation of cardiac assist device within 72 hours
SecondaryStroke6 monthsStroke within 6 months
SecondaryMortality6 monthsAll-cause mortality within 6 months
SecondaryRehospitalization6 monthsHeart failure rehospitalization within 6 months
SecondaryWorsening heart failure≥12 hoursWorsening in-hospital heart failure after PCI
SecondaryComposite≥12 hours or 6 monthsComposite of any worsening in-hospital heart failure ≥12 hours after PCI or heart failure rehospitalization within 6 months

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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