ID

11709

Description

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

Lien

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

Mots-clés

Versions (1)
  1. 28/07/2015 28/07/2015 -
Téléchargé le

28 juillet 2015

DOI

Pour une demande vous connecter.

Licence

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

Anglais

Eligibility criteria

1 Formulaires  
  1. StudyEvent: ODM
    1. Eligibility criteria
Inclusion Criteria
Description

Inclusion Criteria

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

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

Type de données

boolean

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

diagnosis of ST-elevation myocardial infarction

Type de données

boolean

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

diagnosis non-ST elevation myocardial infarction

Type de données

boolean

Alias
UMLS CUI-1
C3537184
diagnosis of unstable angina
Description

diagnosis of unstable angina

Type de données

boolean

Alias
UMLS CUI-1
C0002965
Exclusion Criteria
Description

Exclusion Criteria

Active bleeding
Description

Active bleeding

Type de données

boolean

Alias
UMLS CUI-1
C0019080
risk of bleeding
Description

risk of bleeding

Type de données

boolean

Alias
UMLS CUI-1
C3251812
intracranial hemorrhage
Description

intracranial hemorrhage

Type de données

boolean

Alias
UMLS CUI-1
C0151699
anticoagulant therapy
Description

anticoagulant therapy

Type de données

boolean

Alias
UMLS CUI-1
C0150457
Significantly impaired renal function
Description

Significantly impaired renal function

Type de données

boolean

Alias
UMLS CUI-1
C0035078
Significantly impaired hepatic function
Description

Significantly impaired hepatic function

Type de données

boolean

Alias
UMLS CUI-1
C0085605
cardiogenic shock
Description

cardiogenic shock

Type de données

boolean

Alias
UMLS CUI-1
C0036980
ventricular arrhythmias
Description

ventricular arrhythmias

Type de données

boolean

Alias
UMLS CUI-1
C0085612
Retour au début de la page

Similar models

Eligibility criteria

1 Formulaires
  1. StudyEvent: ODM
    1. Eligibility criteria
Name
Type
Description | Question | Decode (Coded Value)
Type de données
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)
Retour au début de la page 

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