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Eligibility Coronary Artery Disease NCT00474565

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. male and female patients that have an abnormal nuclear medicine heart scan and are already scheduled for cardiac catheterization for evaluation of coronary artery disease or disease of coronary artery bypass grafts will be asked to participate in this trial.
Description

Heart Radionuclide Imaging Abnormal | Cardiac Catheterization Scheduled | Coronary Artery Disease Evaluation | Coronary Artery Bypass Surgery

Data type

boolean

Alias
UMLS CUI [1,1]
C0018787
UMLS CUI [1,2]
C0034606
UMLS CUI [1,3]
C0205161
UMLS CUI [2,1]
C0018795
UMLS CUI [2,2]
C0205539
UMLS CUI [3,1]
C1956346
UMLS CUI [3,2]
C1261322
UMLS CUI [4]
C0010055
2. provided informed consent.
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
3. evaluation by a cardiology division staff or cardiology nurse clinician.
Description

Evaluation

Data type

boolean

Alias
UMLS CUI [1]
C0220825
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. patient is currently enrolled in another related research study.
Description

Study Subject Participation Status | Research study Related

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2,1]
C0681814
UMLS CUI [2,2]
C0439849
2. less than 18 years of age.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
3. pregnant patients.
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
4. abnormal renal function with creatinine equal to or greater than 1.6 mg/dl or those subjects requiring dialysis.
Description

Abnormal renal function | Creatinine measurement, serum | Dialysis Patient need for

Data type

boolean

Alias
UMLS CUI [1]
C0151746
UMLS CUI [2]
C0201976
UMLS CUI [3,1]
C0011946
UMLS CUI [3,2]
C0686904
5. patients with chronic obstructive pulmonary disease or heart-failure with cardiac ejection-fraction less than 30%.
Description

Chronic Obstructive Airway Disease | Heart failure | Cardiac ejection fraction

Data type

boolean

Alias
UMLS CUI [1]
C0024117
UMLS CUI [2]
C0018801
UMLS CUI [3]
C0232174
6. patients with known sensitivity to beta-blockers (lopressor) or have asthma.
Description

Hypersensitivity Adrenergic beta-Antagonists | Hypersensitivity Lopressor | Asthma

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0001645
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0700776
UMLS CUI [3]
C0004096
7. patients receiving an abnormally large volume of contrast media during cardiac catheterization (> 200cc)
Description

Contrast Media Large Abnormal | Cardiac Catheterization

Data type

boolean

Alias
UMLS CUI [1,1]
C0009924
UMLS CUI [1,2]
C0549177
UMLS CUI [1,3]
C0205161
UMLS CUI [2]
C0018795
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Similar models

Eligibility Coronary Artery Disease NCT00474565

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Heart Radionuclide Imaging Abnormal | Cardiac Catheterization Scheduled | Coronary Artery Disease Evaluation | Coronary Artery Bypass Surgery
Item
1. male and female patients that have an abnormal nuclear medicine heart scan and are already scheduled for cardiac catheterization for evaluation of coronary artery disease or disease of coronary artery bypass grafts will be asked to participate in this trial.
boolean
C0018787 (UMLS CUI [1,1])
C0034606 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,3])
C0018795 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
C1956346 (UMLS CUI [3,1])
C1261322 (UMLS CUI [3,2])
C0010055 (UMLS CUI [4])
Informed Consent
Item
2. provided informed consent.
boolean
C0021430 (UMLS CUI [1])
Evaluation
Item
3. evaluation by a cardiology division staff or cardiology nurse clinician.
boolean
C0220825 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Study Subject Participation Status | Research study Related
Item
1. patient is currently enrolled in another related research study.
boolean
C2348568 (UMLS CUI [1])
C0681814 (UMLS CUI [2,1])
C0439849 (UMLS CUI [2,2])
Age
Item
2. less than 18 years of age.
boolean
C0001779 (UMLS CUI [1])
Pregnancy
Item
3. pregnant patients.
boolean
C0032961 (UMLS CUI [1])
Abnormal renal function | Creatinine measurement, serum | Dialysis Patient need for
Item
4. abnormal renal function with creatinine equal to or greater than 1.6 mg/dl or those subjects requiring dialysis.
boolean
C0151746 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
C0011946 (UMLS CUI [3,1])
C0686904 (UMLS CUI [3,2])
Chronic Obstructive Airway Disease | Heart failure | Cardiac ejection fraction
Item
5. patients with chronic obstructive pulmonary disease or heart-failure with cardiac ejection-fraction less than 30%.
boolean
C0024117 (UMLS CUI [1])
C0018801 (UMLS CUI [2])
C0232174 (UMLS CUI [3])
Hypersensitivity Adrenergic beta-Antagonists | Hypersensitivity Lopressor | Asthma
Item
6. patients with known sensitivity to beta-blockers (lopressor) or have asthma.
boolean
C0020517 (UMLS CUI [1,1])
C0001645 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0700776 (UMLS CUI [2,2])
C0004096 (UMLS CUI [3])
Contrast Media Large Abnormal | Cardiac Catheterization
Item
7. patients receiving an abnormally large volume of contrast media during cardiac catheterization (> 200cc)
boolean
C0009924 (UMLS CUI [1,1])
C0549177 (UMLS CUI [1,2])
C0205161 (UMLS CUI [1,3])
C0018795 (UMLS CUI [2])
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