Eligibiltiy Critera

  1. StudyEvent: ODM
    1. Eligibiltiy Critera
Inclusion Criteria
Beschreibung

Inclusion Criteria

A person who has been diagnosed with acute coronary syndrome (ACS) and is to undergo a percutaneous coronary intervention (PCI)
Beschreibung

A person who has been diagnosed with acute coronary syndrome (ACS) and is to undergo a percutaneous coronary intervention (PCI)

Datentyp

boolean

Alias
UMLS CUI-1
C0948089
A person who has been diagnosed with acute coronary syndrome (ACS) and is to undergo a percutaneous coronary intervention (PCI)
Beschreibung

A person who has been diagnosed with acute coronary syndrome (ACS) and is to undergo a percutaneous coronary intervention (PCI)

Datentyp

boolean

Alias
UMLS CUI-1
C1532338
A person who is of East or Southeast Asian descent
Beschreibung

A person who is of East or Southeast Asian descent

Datentyp

boolean

Alias
UMLS CUI-1
C0078988
A person who is of the legal age of 18 (or age 21 in Singapore)
Beschreibung

A person who is of the legal age of 18 (or age 21 in Singapore)

Datentyp

boolean

Alias
UMLS CUI-1
C0001779
Is mentally competent to provide a signed written informed consent before entering the study
Beschreibung

Is mentally competent to provide a signed written informed consent before entering the study

Datentyp

boolean

Alias
UMLS CUI-1
C0021430
If a woman is of childbearing potential, she must test negative for pregnancy
Beschreibung

If a woman is of childbearing potential, she must test negative for pregnancy

Datentyp

boolean

Alias
UMLS CUI-1
C0549206
agree to use a reliable method of birth control
Beschreibung

agree to use a reliable method of birth control

Datentyp

boolean

Alias
UMLS CUI-1
C0700589
Exclusion Criteria
Beschreibung

Exclusion Criteria

cardiogenic shock
Beschreibung

cardiogenic shock

Datentyp

boolean

Alias
UMLS CUI-1
C0036980
ventricular arrhythmias
Beschreibung

ventricular arrhythmias

Datentyp

boolean

Alias
UMLS CUI-1
C0085612
congestive heart failure
Beschreibung

congestive heart failure

Datentyp

boolean

Alias
UMLS CUI-1
C0018802
A person who is at an increased risk of bleeding (e.g. active internal bleeding, history of bleeding disorder, recent fibrinolytic therapy before randomization into the study)
Beschreibung

A person who is at an increased risk of bleeding (e.g. active internal bleeding, history of bleeding disorder, recent fibrinolytic therapy before randomization into the study)

Datentyp

boolean

Alias
UMLS CUI-1
C3251812
History of ischemic or hemorrhagic stroke
Beschreibung

History of ischemic or hemorrhagic stroke

Datentyp

boolean

Alias
UMLS CUI-1
C0559159
intracranial neoplasm
Beschreibung

intracranial neoplasm

Datentyp

boolean

Alias
UMLS CUI-1
C1527390
arteriovenous malformation
Beschreibung

arteriovenous malformation

Datentyp

boolean

Alias
UMLS CUI-1
C0003857
aneurysm
Beschreibung

aneurysm

Datentyp

boolean

prior history of transient ischemic attack (TIA)
Beschreibung

prior history of transient ischemic attack (TIA)

Datentyp

boolean

Alias
UMLS CUI-1
C0455536
A person who needs to take other antiplatelet therapy other than Aspirin for the duration of the study
Beschreibung

A person who needs to take other antiplatelet therapy other than Aspirin for the duration of the study

Datentyp

boolean

Alias
UMLS CUI-1
C1096021
A person who receives daily treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) or cyclooxygenase-2 (COX2) inhibitors that cannot be discontinued
Beschreibung

A person who receives daily treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) or cyclooxygenase-2 (COX2) inhibitors that cannot be discontinued

Datentyp

boolean

Alias
UMLS CUI-1
C0003211
A person who has a severe liver disease, such as cirrhosis
Beschreibung

A person who has a severe liver disease, such as cirrhosis

Datentyp

boolean

Alias
UMLS CUI-1
C0085605
Alcoholism
Beschreibung

Alcoholism

Datentyp

boolean

Alias
UMLS CUI-1
C0455500
mental illness
Beschreibung

mental illness

Datentyp

boolean

Alias
UMLS CUI-1
C0004936
drug dependence
Beschreibung

drug dependence

Datentyp

boolean

Alias
UMLS CUI-1
C1510472

Ähnliche Modelle

Eligibiltiy Critera

  1. StudyEvent: ODM
    1. Eligibiltiy Critera
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
Inclusion Criteria
Acute coronary syndrome
Item
A person who has been diagnosed with acute coronary syndrome (ACS) and is to undergo a percutaneous coronary intervention (PCI)
boolean
C0948089 (UMLS CUI-1)
PCI
Item
A person who has been diagnosed with acute coronary syndrome (ACS) and is to undergo a percutaneous coronary intervention (PCI)
boolean
C1532338 (UMLS CUI-1)
Asian
Item
A person who is of East or Southeast Asian descent
boolean
C0078988 (UMLS CUI-1)
Age
Item
A person who is of the legal age of 18 (or age 21 in Singapore)
boolean
C0001779 (UMLS CUI-1)
Informed consent
Item
Is mentally competent to provide a signed written informed consent before entering the study
boolean
C0021430 (UMLS CUI-1)
Pregnancy
Item
If a woman is of childbearing potential, she must test negative for pregnancy
boolean
C0549206 (UMLS CUI-1)
Birth control
Item
agree to use a reliable method of birth control
boolean
C0700589 (UMLS CUI-1)
Item Group
Exclusion Criteria
cardiogenic shock
Item
cardiogenic shock
boolean
C0036980 (UMLS CUI-1)
ventricular arrhythmia
Item
ventricular arrhythmias
boolean
C0085612 (UMLS CUI-1)
congestive heart failure
Item
congestive heart failure
boolean
C0018802 (UMLS CUI-1)
Bleeding risk
Item
A person who is at an increased risk of bleeding (e.g. active internal bleeding, history of bleeding disorder, recent fibrinolytic therapy before randomization into the study)
boolean
C3251812 (UMLS CUI-1)
History of stroke
Item
History of ischemic or hemorrhagic stroke
boolean
C0559159 (UMLS CUI-1)
intracranial neoplasm
Item
intracranial neoplasm
boolean
C1527390 (UMLS CUI-1)
arteriovenous malformation
Item
arteriovenous malformation
boolean
C0003857 (UMLS CUI-1)
aneurysm
Item
aneurysm
boolean
History of TIA
Item
prior history of transient ischemic attack (TIA)
boolean
C0455536 (UMLS CUI-1)
antiplatelet therapy
Item
A person who needs to take other antiplatelet therapy other than Aspirin for the duration of the study
boolean
C1096021 (UMLS CUI-1)
NSAID
Item
A person who receives daily treatment with nonsteroidal anti-inflammatory drugs (NSAIDs) or cyclooxygenase-2 (COX2) inhibitors that cannot be discontinued
boolean
C0003211 (UMLS CUI-1)
liver failure
Item
A person who has a severe liver disease, such as cirrhosis
boolean
C0085605 (UMLS CUI-1)
Alcoholism
Item
Alcoholism
boolean
C0455500 (UMLS CUI-1)
mental disorders
Item
mental illness
boolean
C0004936 (UMLS CUI-1)
drug dependence
Item
drug dependence
boolean
C1510472 (UMLS CUI-1)