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Eligibility Coronary Artery Disease NCT00765908

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
ability to give written informed consent.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
all patients who are listed for elective pci of at least one major epicardial artery.
Description

Percutaneous Coronary Intervention elective Scheduled | Artery Epicardial Major Quantity

Data type

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0439608
UMLS CUI [1,3]
C0205539
UMLS CUI [2,1]
C0003842
UMLS CUI [2,2]
C0442016
UMLS CUI [2,3]
C0205164
UMLS CUI [2,4]
C1265611
patients ≥ 18 years and ≤80 years of age.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
any patient who has experienced chest pain within the preceding 24 hrs
Description

Chest Pain

Data type

boolean

Alias
UMLS CUI [1]
C0008031
any patient who exhibits haemodynamic instability (systolic bp <90mmhg, pulmonary oedema);
Description

Hemodynamic instability | Systolic Pressure | Pulmonary Edema

Data type

boolean

Alias
UMLS CUI [1]
C0948268
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0034063
any patient with electrophysiologic instability (arrythmias eg rapid af) or an abnormal baseline electrocardiogram (ecg) (e.g., significant st segment depression, left bundle-branch block) which precludes analysis of the st segment shift during pci
Description

Electrophysiological Processes Instability | Cardiac Arrhythmia | Rapid atrial fibrillation | Electrocardiogram abnormal | ST segment depression | Left Bundle-Branch Block | Preventing Analysis ST segment changes During Percutaneous Coronary Intervention

Data type

boolean

Alias
UMLS CUI [1,1]
C2350528
UMLS CUI [1,2]
C1444783
UMLS CUI [2]
C0003811
UMLS CUI [3]
C1281999
UMLS CUI [4]
C0522055
UMLS CUI [5]
C0520887
UMLS CUI [6]
C0023211
UMLS CUI [7,1]
C1292733
UMLS CUI [7,2]
C0936012
UMLS CUI [7,3]
C0232326
UMLS CUI [7,4]
C0347984
UMLS CUI [7,5]
C1532338
patients unable to give informed consent
Description

Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
previous inclusion in this or any other clinical trial within one month prior to inclusion.
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
diabetes
Description

Diabetes Mellitus

Data type

boolean

Alias
UMLS CUI [1]
C0011849
uncontrolled hypertension (bp>180/110).
Description

Uncontrolled hypertension | Blood pressure measurement

Data type

boolean

Alias
UMLS CUI [1]
C1868885
UMLS CUI [2]
C0005824
anaemia (hb <10g/l).
Description

Anemia | Hemoglobin measurement

Data type

boolean

Alias
UMLS CUI [1]
C0002871
UMLS CUI [2]
C0518015
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Similar models

Eligibility Coronary Artery Disease NCT00765908

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
ability to give written informed consent.
boolean
C0021430 (UMLS CUI [1])
Percutaneous Coronary Intervention elective Scheduled | Artery Epicardial Major Quantity
Item
all patients who are listed for elective pci of at least one major epicardial artery.
boolean
C1532338 (UMLS CUI [1,1])
C0439608 (UMLS CUI [1,2])
C0205539 (UMLS CUI [1,3])
C0003842 (UMLS CUI [2,1])
C0442016 (UMLS CUI [2,2])
C0205164 (UMLS CUI [2,3])
C1265611 (UMLS CUI [2,4])
Age
Item
patients ≥ 18 years and ≤80 years of age.
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Chest Pain
Item
any patient who has experienced chest pain within the preceding 24 hrs
boolean
C0008031 (UMLS CUI [1])
Hemodynamic instability | Systolic Pressure | Pulmonary Edema
Item
any patient who exhibits haemodynamic instability (systolic bp <90mmhg, pulmonary oedema);
boolean
C0948268 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0034063 (UMLS CUI [3])
Electrophysiological Processes Instability | Cardiac Arrhythmia | Rapid atrial fibrillation | Electrocardiogram abnormal | ST segment depression | Left Bundle-Branch Block | Preventing Analysis ST segment changes During Percutaneous Coronary Intervention
Item
any patient with electrophysiologic instability (arrythmias eg rapid af) or an abnormal baseline electrocardiogram (ecg) (e.g., significant st segment depression, left bundle-branch block) which precludes analysis of the st segment shift during pci
boolean
C2350528 (UMLS CUI [1,1])
C1444783 (UMLS CUI [1,2])
C0003811 (UMLS CUI [2])
C1281999 (UMLS CUI [3])
C0522055 (UMLS CUI [4])
C0520887 (UMLS CUI [5])
C0023211 (UMLS CUI [6])
C1292733 (UMLS CUI [7,1])
C0936012 (UMLS CUI [7,2])
C0232326 (UMLS CUI [7,3])
C0347984 (UMLS CUI [7,4])
C1532338 (UMLS CUI [7,5])
Informed Consent Unable
Item
patients unable to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Study Subject Participation Status
Item
previous inclusion in this or any other clinical trial within one month prior to inclusion.
boolean
C2348568 (UMLS CUI [1])
Diabetes Mellitus
Item
diabetes
boolean
C0011849 (UMLS CUI [1])
Uncontrolled hypertension | Blood pressure measurement
Item
uncontrolled hypertension (bp>180/110).
boolean
C1868885 (UMLS CUI [1])
C0005824 (UMLS CUI [2])
Anemia | Hemoglobin measurement
Item
anaemia (hb <10g/l).
boolean
C0002871 (UMLS CUI [1])
C0518015 (UMLS CUI [2])
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