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Trial · NCT00623623

Registered outcomes25

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

ListOutcomeTime frameDescription
PrimaryNumber of Patients With All-cause Mortality, Cardiogenic Shock, Congestive Heart Failure and Recurrent Myocardial Infarction Within 30 Days for FAS.30 daysThe number of observed patients with all-cause mortality, cardiogenic shock, congestive heart failure (CHF) and recurrent myocardial infarction within 30 days was reported for full analysis set (FAS).
SecondaryNumber of Patients With All Cause Mortality30 daysThis is a key secondary endpoint. The number of observed patients with all cause mortality within 30 days was reported.
SecondaryNumber of Patients With Cardiac Mortality30 daysThis is a key secondary endpoint. The number of observed patients with cardiac mortality within 30 days was reported.
SecondaryNumber of Patients With Cardiogenic Shock30 daysThis is a key secondary endpoint. The number of observed patients with cardiogenic shock within 30 days was reported.
SecondaryNumber of Patients With Congestive Heart Failure (CHF)30 daysThis is a key secondary endpoint. The number of observed patients with congestive heart failure (CHF) within 30 days was reported.
SecondaryNumber of Patients With Recurrent Myocardial Infarction (Reinfarction)30 daysThis is a key secondary endpoint. The number of observed patients with recurrent myocardial infarction (reinfarction) within 30 days was reported
SecondaryNumber of Patients With Rehospitalisation for Cardiac Reasons30 daysThis is a key secondary endpoint. The number of observed patients with rehospitalisation for cardiac reasons within 30 days was reported
SecondaryNumber of Patients With Rehospitalisation for Non-cardiac Reasons30 daysThis is a key secondary endpoint. The number of observed patients with rehospitalisation for non-cardiac reasons within 30 days was reported
SecondaryNumber of Patients With Serious Repeat Target Vessel Revascularization30 daysThis is a key secondary endpoint. The number of observed patients with serious repeat target vessel revascularization within 30 days was reported
SecondaryNumber of Patients With All Cause Death and Shock30 daysThis is a key secondary endpoint. The number of observed patients with all cause death and shock within 30 days was reported
SecondaryNumber of Patients With All Cause Death and Shock and CHF30 daysThis is a key secondary endpoint. The number of observed patients with all cause death and shock and CHF within 30 days was reported.
SecondaryNumber of Patients With All Cause Death and Shock and Reinfarction30 daysThis is a key secondary endpoint. The number of observed patients with all cause death and shock and reinfarction within 30 days was reported
SecondaryNumber of Patients With Total Fatal Stroke30 daysThis is a key secondary endpoint. The number of observed patients with total fatal stroke within 30 days was reported
SecondaryNumber of Patients With Total Disabling Stroke30 daysThis is a key secondary endpoint. The number of observed patients with total disabling stroke within 30 days was reported
SecondaryNumber of Patients With Total Non-disabling Stroke30 daysThis is a key secondary endpoint. The number of observed patients with total non-disabling stroke within 30 days was reported
SecondaryNumber of Patients With Intracranial Haemorrhage30 daysThis is a key secondary endpoint. The number of observed patients with intracranial haemorrhage within 30 days was reported
SecondaryNumber of Patients With Ischaemic Stroke30 daysThis is a key secondary endpoint. The number of observed patients with ischaemic stroke within 30 days was reported
SecondaryNumber of Patients With Total Stroke (All Types)30 daysThis is a key secondary endpoint. The number of observed patients with total stroke (all types) within 30 days was reported
SecondaryNumber of Patients With Major Non-intracranial Bleeds Including Blood Transfusions30 daysThis is a key secondary endpoint. The number of observed patients with major non-intracranial bleeds including blood transfusions within 30 days was reported
SecondaryNumber of Patients With Minor Non-intracranial Bleeds30 daysThis is a key secondary endpoint. The number of observed patients with minor non-intracranial bleeds within 30 days was reported

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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