Eligibility Contrast Induced Nephropathy NCT01061320

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
serum creatinine levels > 1.2 mg/dl and baseline creatinine clearance levels < 60 ml/min (as measured in their most recent sample,drawn within 2 months prior to the beginning of the study)
Description

Creatinine measurement, serum | Creatinine clearance measurement

Data type

boolean

Alias
UMLS CUI [1]
C0201976
UMLS CUI [2]
C0373595
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with acute kidney injury
Description

Injury of kidney

Data type

boolean

Alias
UMLS CUI [1]
C0160420
end stage renal disease (requiring dialysis)
Description

End stage renal disease | Requirement Dialysis

Data type

boolean

Alias
UMLS CUI [1]
C0022661
UMLS CUI [2,1]
C1514873
UMLS CUI [2,2]
C0011946
unstable renal function (as evidenced by a change in serum creatinine of > 0.5 mg/dl, or > 25%, within 14 days prior to the study)
Description

Renal function Unstable | Change Serum creatinine

Data type

boolean

Alias
UMLS CUI [1,1]
C0232804
UMLS CUI [1,2]
C0443343
UMLS CUI [2,1]
C0392747
UMLS CUI [2,2]
C0600061
allergy to any of the contrast agents
Description

Contrast media allergy

Data type

boolean

Alias
UMLS CUI [1]
C0570562
mechanical ventilation
Description

Mechanical ventilation

Data type

boolean

Alias
UMLS CUI [1]
C0199470
suffered from congestive heart failure, cardiogenic shock or emergent angiography.
Description

Congestive heart failure | Shock, Cardiogenic | Emergency angiography

Data type

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2]
C0036980
UMLS CUI [3,1]
C0013956
UMLS CUI [3,2]
C0002978
receiving nac, mannitol, diuretics, theophylline, dopamine, vitamin e or contrast agents within 14 days before the study
Description

Acetylcysteine | Mannitol | Diuretics | Theophylline | Dopamine | Vitamin E | Contrast Media

Data type

boolean

Alias
UMLS CUI [1]
C0001047
UMLS CUI [2]
C0024730
UMLS CUI [3]
C0012798
UMLS CUI [4]
C0039771
UMLS CUI [5]
C0013030
UMLS CUI [6]
C0042874
UMLS CUI [7]
C0009924

Similar models

Eligibility Contrast Induced Nephropathy NCT01061320

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Creatinine measurement, serum | Creatinine clearance measurement
Item
serum creatinine levels > 1.2 mg/dl and baseline creatinine clearance levels < 60 ml/min (as measured in their most recent sample,drawn within 2 months prior to the beginning of the study)
boolean
C0201976 (UMLS CUI [1])
C0373595 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Injury of kidney
Item
patients with acute kidney injury
boolean
C0160420 (UMLS CUI [1])
End stage renal disease | Requirement Dialysis
Item
end stage renal disease (requiring dialysis)
boolean
C0022661 (UMLS CUI [1])
C1514873 (UMLS CUI [2,1])
C0011946 (UMLS CUI [2,2])
Renal function Unstable | Change Serum creatinine
Item
unstable renal function (as evidenced by a change in serum creatinine of > 0.5 mg/dl, or > 25%, within 14 days prior to the study)
boolean
C0232804 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0392747 (UMLS CUI [2,1])
C0600061 (UMLS CUI [2,2])
Contrast media allergy
Item
allergy to any of the contrast agents
boolean
C0570562 (UMLS CUI [1])
Mechanical ventilation
Item
mechanical ventilation
boolean
C0199470 (UMLS CUI [1])
Congestive heart failure | Shock, Cardiogenic | Emergency angiography
Item
suffered from congestive heart failure, cardiogenic shock or emergent angiography.
boolean
C0018802 (UMLS CUI [1])
C0036980 (UMLS CUI [2])
C0013956 (UMLS CUI [3,1])
C0002978 (UMLS CUI [3,2])
Acetylcysteine | Mannitol | Diuretics | Theophylline | Dopamine | Vitamin E | Contrast Media
Item
receiving nac, mannitol, diuretics, theophylline, dopamine, vitamin e or contrast agents within 14 days before the study
boolean
C0001047 (UMLS CUI [1])
C0024730 (UMLS CUI [2])
C0012798 (UMLS CUI [3])
C0039771 (UMLS CUI [4])
C0013030 (UMLS CUI [5])
C0042874 (UMLS CUI [6])
C0009924 (UMLS CUI [7])