ID

11708

Beskrivning

The purpose of this study is to determine whether rivaroxaban in addition to standard care reduces the risk of the composite of cardiovascular death, myocardial infarction, or stroke in patients with a recent acute coronary syndrome compared with placebo. https://clinicaltrials.gov/ct2/show/NCT00809965

Länk

https://clinicaltrials.gov/ct2/show/NCT00809965

Nyckelord

  1. 2015-07-28 2015-07-28 -
Uppladdad den

28 juli 2015

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Rivaroxaban Acute Coronary Syndrome NCT00809965

Elegibility Criteria

  1. StudyEvent: ODM
    1. Elegibility Criteria
Inclusion Criteria
Beskrivning

Inclusion Criteria

Currently receiving aspirin
Beskrivning

Currently receiving aspirin

Datatyp

boolean

Alias
UMLS CUI-1
C0004057
Hospitalized with symptoms suggestive of acute coronary syndrome
Beskrivning

Hospitalized with symptoms suggestive of acute coronary syndrome

Datatyp

boolean

Alias
UMLS CUI-1
C0948089
Exclusion criteria
Beskrivning

Exclusion criteria

Significant renal impairment
Beskrivning

Significant renal impairment

Datatyp

boolean

Alias
UMLS CUI-1
C0035078
Significant liver disease
Beskrivning

Significant liver disease

Datatyp

boolean

Alias
UMLS CUI-1
C0085605
Need for continued anticoagulant therapy
Beskrivning

Need for continued anticoagulant therapy

Datatyp

boolean

Alias
UMLS CUI-1
C0150457
Any condition that, in the opinion of the investigator, contraindicates anticoagulant therapy
Beskrivning

Any condition that, in the opinion of the investigator, contraindicates anticoagulant therapy

Datatyp

boolean

Alias
UMLS CUI-1
C1531588

Similar models

Elegibility Criteria

  1. StudyEvent: ODM
    1. Elegibility Criteria
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
Inclusion Criteria
Aspirin
Item
Currently receiving aspirin
boolean
C0004057 (UMLS CUI-1)
Acute coronary syndrome
Item
Hospitalized with symptoms suggestive of acute coronary syndrome
boolean
C0948089 (UMLS CUI-1)
Item Group
Exclusion criteria
Kidney failure
Item
Significant renal impairment
boolean
C0035078 (UMLS CUI-1)
Liver failure
Item
Significant liver disease
boolean
C0085605 (UMLS CUI-1)
Anticoagulant therapy
Item
Need for continued anticoagulant therapy
boolean
C0150457 (UMLS CUI-1)
Anticoagulant contraindicated
Item
Any condition that, in the opinion of the investigator, contraindicates anticoagulant therapy
boolean
C1531588 (UMLS CUI-1)

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