Eligibility Acute Coronary Syndrome NCT01498731 DRKS00000276

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI-1
C1512693
Typical chest pain (with or without ECG-changes, but no ST-elevation)suggestive of unstable angina or non-ST-elevated myocardial infarction (NSTEMI)
Description

Chest Pain

Data type

boolean

Alias
UMLS CUI [1]
C0008031
Troponin negative at admission according to the current clinical practice Patient willing and able to give written informed consent
Description

Troponin

Data type

boolean

Alias
UMLS CUI [1]
C0523952
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI-1
C0680251
Healthy Volunteers
Description

Control Group

Data type

boolean

Alias
UMLS CUI [1]
C0009932
Patients with ST-elevation myocardial infarction (STEMI)
Description

ST-elevation myocardial infarction

Data type

boolean

Alias
UMLS CUI [1]
C1536220
Continuing chest pain or recurrent episodes of chest pain under therapy
Description

Chest Pain Specification

Data type

boolean

Alias
UMLS CUI [1,1]
C0008031
UMLS CUI [1,2]
C2348235
High-risk patients with suspected ACS who need to be hospitalized for reasons independent of their initial troponin result
Description

Hospitalization

Data type

boolean

Alias
UMLS CUI [1]
C0019993
Patients who need to be hospitalized for other medical reasons
Description

Hospitalization for other medical reasons

Data type

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C3841427
Patients in need of urgent life-saving interventions
Description

Requires immediate life-saving intervention

Data type

boolean

Alias
UMLS CUI [1]
C4264611
Patients under 18 years of age
Description

Age

Data type

boolean

Patients with a life expectancy < 6 months
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
Patients with any condition that leads the treating physician to not consider the patient eligible for the trial
Description

Eligibility Determination

Data type

boolean

Alias
UMLS CUI [1]
C0013893

Similar models

Eligibility Acute Coronary Syndrome NCT01498731 DRKS00000276

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion Criteria
C1512693 (UMLS CUI-1)
Chest Pain
Item
Typical chest pain (with or without ECG-changes, but no ST-elevation)suggestive of unstable angina or non-ST-elevated myocardial infarction (NSTEMI)
boolean
C0008031 (UMLS CUI [1])
Troponin
Item
Troponin negative at admission according to the current clinical practice Patient willing and able to give written informed consent
boolean
C0523952 (UMLS CUI [1])
Item Group
Exclusion Criteria
C0680251 (UMLS CUI-1)
Control Group
Item
Healthy Volunteers
boolean
C0009932 (UMLS CUI [1])
ST-elevation myocardial infarction
Item
Patients with ST-elevation myocardial infarction (STEMI)
boolean
C1536220 (UMLS CUI [1])
Chest Pain Specification
Item
Continuing chest pain or recurrent episodes of chest pain under therapy
boolean
C0008031 (UMLS CUI [1,1])
C2348235 (UMLS CUI [1,2])
Hospitalization
Item
High-risk patients with suspected ACS who need to be hospitalized for reasons independent of their initial troponin result
boolean
C0019993 (UMLS CUI [1])
Hospitalization for other medical reasons
Item
Patients who need to be hospitalized for other medical reasons
boolean
C0019993 (UMLS CUI [1,1])
C3841427 (UMLS CUI [1,2])
Requires immediate life-saving intervention
Item
Patients in need of urgent life-saving interventions
boolean
C4264611 (UMLS CUI [1])
Age
Item
Patients under 18 years of age
boolean
Life Expectancy
Item
Patients with a life expectancy < 6 months
boolean
C0023671 (UMLS CUI [1])
Eligibility Determination
Item
Patients with any condition that leads the treating physician to not consider the patient eligible for the trial
boolean
C0013893 (UMLS CUI [1])