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Trial · NCT00502528

Registered outcomes11

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

ListOutcomeTime frameDescription
PrimaryMyocardial perfusion determined by CMR3 days
SecondaryFinal infarct size determined by CMR3 days
SecondaryLeft ventricular function determined by CMR3 days/ 6 months (6-months Remodeling-substudy)
SecondaryPlasma NT-BNP30 days/ 6 months (6-months substudy)
SecondaryEnzymatic infarct size (CK levels)3 days
SecondaryECG ST-segment resolution1 hour
SecondaryMarkers of inflammation24 hours/ 30 days
SecondaryMajor adverse cardiac events (MACE) (cardiovascular death, re-hospitalization for unstable angina and AMI, hospitalization for worsening heart failure)30 days
SecondaryLiver function24hours/ 3 days/ 30 days
SecondaryEvent free survival6 months (6-months substudy)
SecondaryHolter ECG3 days / 30 days (EP-substudy)

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.

For software

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Twenty rows a page, as JSON. No key.

GET https://conductscience.org/api/trials/v1/NCT00502528/registered