Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Inclusion Criteria
Beschreibung

Inclusion Criteria

Male or female outpatients
Beschreibung

Male or female outpatients

Datentyp

boolean

Alias
UMLS CUI-1
C0079399
18 years old or older
Beschreibung

18 years old or older

Datentyp

boolean

Alias
UMLS CUI-1
C0001779
Final diagnosis of acute coronary syndrome
Beschreibung

Final diagnosis of acute coronary syndrome

Datentyp

boolean

Alias
UMLS CUI-1
C0948089
ischemic chest discomfort
Beschreibung

ischemic chest discomfort

Datentyp

boolean

Alias
UMLS CUI-1
C0008031
Elevated concentrations of natriuretic peptide 3-10 days after admission for their qualifying acute coronary syndrome event
Beschreibung

Elevated concentrations of natriuretic peptide 3-10 days after admission for their qualifying acute coronary syndrome event

Datentyp

boolean

Alias
UMLS CUI-1
C1095989
Exclusion criteria
Beschreibung

Exclusion criteria

Presence of clinically overt heart failure
Beschreibung

Presence of clinically overt heart failure

Datentyp

boolean

Alias
UMLS CUI-1
C0018801
Known evidence of left ventricular systolic dysfunction
Beschreibung

Known evidence of left ventricular systolic dysfunction

Datentyp

boolean

Alias
UMLS CUI-1
C1277187
Percutaneous coronary intervention (PCI) less than 24 hours before randomization
Beschreibung

Percutaneous coronary intervention (PCI) less than 24 hours before randomization

Datentyp

boolean

Alias
UMLS CUI-1
C1532338
chronic ACEI therapy
Beschreibung

chronic ACEI therapy

Datentyp

boolean

Alias
UMLS CUI-1
C0003015
chronic ARB therapy
Beschreibung

chronic ARB therapy

Datentyp

boolean

Alias
UMLS CUI-1
C0521942

Ähnliche Modelle

Eligibility Criteria

  1. StudyEvent: ODM
    1. Eligibility Criteria
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Inclusion Criteria
Gender
Item
Male or female outpatients
boolean
C0079399 (UMLS CUI-1)
Age
Item
18 years old or older
boolean
C0001779 (UMLS CUI-1)
Acute coronary syndrome
Item
Final diagnosis of acute coronary syndrome
boolean
C0948089 (UMLS CUI-1)
Chest pain
Item
ischemic chest discomfort
boolean
C0008031 (UMLS CUI-1)
BNP
Item
Elevated concentrations of natriuretic peptide 3-10 days after admission for their qualifying acute coronary syndrome event
boolean
C1095989 (UMLS CUI-1)
Item Group
Exclusion criteria
Heart failure
Item
Presence of clinically overt heart failure
boolean
C0018801 (UMLS CUI-1)
Left ventricular systolic dysfunction
Item
Known evidence of left ventricular systolic dysfunction
boolean
C1277187 (UMLS CUI-1)
PCI
Item
Percutaneous coronary intervention (PCI) less than 24 hours before randomization
boolean
C1532338 (UMLS CUI-1)
ACE inhibitors
Item
chronic ACEI therapy
boolean
C0003015 (UMLS CUI-1)
ARB
Item
chronic ARB therapy
boolean
C0521942 (UMLS CUI-1)