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Trial · NCT03470441

Registered outcomes19

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

ListOutcomeTime frameDescription
PrimaryArrhythmias of Interest, 48 Hours (Overall)First 48 hours post-treatmentNumber of patients experiencing clinically relevant arrhythmias during the first 48 hours post-treatment.
PrimaryArrhythmias of Interest Incidence Rate, 48 Hours (Overall)48 hours post-treatment
Incidence rate of clinically relevant arrhythmias during the first 48 hours post-treatment defined as the number of patients who experienced an arrhythmia divided by the total person-monitoring time within each treatment group
PrimaryArrhythmias of Interest, 14 Days (Overall)48 hours to 14 days Post Percutaneous Coronary Intervention (PCI)Number of patients experiencing clinically relevant arrhythmias 48 hours to 14 days post-treatment.
PrimaryArrhythmias of Interest Incidence Rate, 14 Days (Overall)48 hours to 14 days Post Percutaneous Coronary Intervention (PCI)
Incidence rate of clinically relevant arrhythmias 48 hours to 14 days post-treatment defined as the number of patients who experienced an arrhythmia divided by the total person-monitoring time within each treatment group
SecondaryInfarct Size Relative to Ventricular Volume, 72 Hours (Overall)72 hours post-treatmentInfarct size relative to ventricular volume (INF/VV) at 72 hours post-treatment
SecondaryInfarct Size Relative to Ventricular Volume, 3 Months (Overall)3 months post-treatmentInfarct size relative to ventricular volume (INF/VV) at 3 months post-treatment)
SecondaryInfarct Size Relative to Ventricular Volume, 72 Hours (Anterior Infarcts)72 hours post-treatmentInfarct size relative to ventricular volume (INF/VV) at 72 hours post-treatment)
SecondaryInfarct Size Relative to Ventricular Volume, 3 Months (Anterior Infarcts)3 months post-treatmentInfarct size relative to ventricular volume (INF/VV) at 3 months post-treatment)
SecondaryLeft Ventricular End Systolic Volume Index, 72 Hours (Overall)72 hours post-treatmentLeft ventricular end systolic volume index (LVESVi) at 72 hours post-treatment
SecondaryLeft Ventricular End Systolic Volume Index, 3 Months (Overall)3 months post-treatmentLeft ventricular end systolic volume index (LVESVi) at 3 Months post-treatment
SecondaryLeft Ventricular End Systolic Volume Index, 72 Hours (Anterior Infarcts)72 hours post-treatmentLeft ventricular end systolic volume index (LVESVi) at 72 Hours post-treatment
SecondaryLeft Ventricular End Systolic Volume Index, 3 Months (Anterior Infarcts)3 months post-treatmentLeft ventricular end systolic volume index (LVESVi) at 3 Months post-treatment
SecondaryLeft Ventricular Ejection Fraction, 72 Hours (Overall)72 hours post-treatmentLeft ventricular ejection fraction at 72 hours post-treatment
SecondaryLeft Ventricular Ejection Fraction, 3 Months (Overall)3 months post-treatmentLeft Ventricular Ejection Fraction at 3 Months (Overall)
SecondaryLeft Ventricular Ejection Fraction, 72 Hours (Anterior Infarcts)72 hours post-treatmentLeft ventricular ejection fraction at 72 hours post-treatment
SecondaryLeft Ventricular Ejection Fraction, 3 Months (Anterior Infarcts)3 months post-treatmentLeft Ventricular Ejection Fraction at 3 Months (Anterior Infarcts)
SecondarySerum Troponin Concentrations, 48 Hours (Overall)48 hours post-treatmentArea under the curve of serum troponins measured over 48 hours post-treatment
SecondarySerum Troponin Concentrations, 48 Hours (Anterior Infarcts)48 hours post-treatmentArea under the curve of serum troponins measured over 48 hours post-treatment
SecondaryST-segment Resolution4 hours post-doseProportion of patients with ST-segment resolution at 4 hours post-dose

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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GET https://conductscience.org/api/trials/v1/NCT03470441/registered