ID

11709

Descripción

The purpose of this study is to evaluate the safety of rivaroxaban in patients with recent acute coronary syndrome (ACS) and to assess the ability of rivaroxaban to reduce the occurrence of death, myocardial infarction (heart attack), repeat myocardial infarctions, stroke, and ischemia (inadequate blood supply to a local area) in patients with recent ACS. https://clinicaltrials.gov/ct2/show/NCT00402597

Link

https://clinicaltrials.gov/ct2/show/NCT00402597

Palabras clave

Versiones (1)
  1. 28/7/15 28/7/15 -
Subido en

28 de julio de 2015

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility ATLAS ACS TIMI 46 Acute Coronary Syndrome NCT00402597

Inglés

Eligibility criteria

1 formularios  
  1. StudyEvent: ODM
    1. Eligibility criteria
Inclusion Criteria
Descripción

Inclusion Criteria

Have symptoms suggestive of ACS that lasted at least 10 minutes at rest occurring within 7 days of randomization
Descripción

Have symptoms suggestive of ACS that lasted at least 10 minutes at rest occurring within 7 days of randomization

Tipo de datos

boolean

Alias
UMLS CUI-1
C0948089
diagnosis of ST-elevation myocardial infarction
Descripción

diagnosis of ST-elevation myocardial infarction

Tipo de datos

boolean

Alias
UMLS CUI-1
C1536220
diagnosis non-ST elevation myocardial infarction
Descripción

diagnosis non-ST elevation myocardial infarction

Tipo de datos

boolean

Alias
UMLS CUI-1
C3537184
diagnosis of unstable angina
Descripción

diagnosis of unstable angina

Tipo de datos

boolean

Alias
UMLS CUI-1
C0002965
Exclusion Criteria
Descripción

Exclusion Criteria

Active bleeding
Descripción

Active bleeding

Tipo de datos

boolean

Alias
UMLS CUI-1
C0019080
risk of bleeding
Descripción

risk of bleeding

Tipo de datos

boolean

Alias
UMLS CUI-1
C3251812
intracranial hemorrhage
Descripción

intracranial hemorrhage

Tipo de datos

boolean

Alias
UMLS CUI-1
C0151699
anticoagulant therapy
Descripción

anticoagulant therapy

Tipo de datos

boolean

Alias
UMLS CUI-1
C0150457
Significantly impaired renal function
Descripción

Significantly impaired renal function

Tipo de datos

boolean

Alias
UMLS CUI-1
C0035078
Significantly impaired hepatic function
Descripción

Significantly impaired hepatic function

Tipo de datos

boolean

Alias
UMLS CUI-1
C0085605
cardiogenic shock
Descripción

cardiogenic shock

Tipo de datos

boolean

Alias
UMLS CUI-1
C0036980
ventricular arrhythmias
Descripción

ventricular arrhythmias

Tipo de datos

boolean

Alias
UMLS CUI-1
C0085612
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Similar models

Eligibility criteria

1 formularios
  1. StudyEvent: ODM
    1. Eligibility criteria
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Inclusion Criteria
Acute coronary syndrome
Item
Have symptoms suggestive of ACS that lasted at least 10 minutes at rest occurring within 7 days of randomization
boolean
C0948089 (UMLS CUI-1)
STEMI
Item
diagnosis of ST-elevation myocardial infarction
boolean
C1536220 (UMLS CUI-1)
NSTEMI
Item
diagnosis non-ST elevation myocardial infarction
boolean
C3537184 (UMLS CUI-1)
Unstable angina
Item
diagnosis of unstable angina
boolean
C0002965 (UMLS CUI-1)
Item Group
Exclusion Criteria
Hemorrhage
Item
Active bleeding
boolean
C0019080 (UMLS CUI-1)
Bleeding risk
Item
risk of bleeding
boolean
C3251812 (UMLS CUI-1)
intracranial hemorrhage
Item
intracranial hemorrhage
boolean
C0151699 (UMLS CUI-1)
anticoagulant therapy
Item
anticoagulant therapy
boolean
C0150457 (UMLS CUI-1)
Kidney failure
Item
Significantly impaired renal function
boolean
C0035078 (UMLS CUI-1)
Liver failure
Item
Significantly impaired hepatic function
boolean
C0085605 (UMLS CUI-1)
cardiogenic shock
Item
cardiogenic shock
boolean
C0036980 (UMLS CUI-1)
ventricular arrhythmia
Item
ventricular arrhythmias
boolean
C0085612 (UMLS CUI-1)
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