ID

28426

Description

Renoprotective Effects of Fluid Prophylaxis Strategies for Contrast Induced Nephropathy (CIN); ODM derived from: https://clinicaltrials.gov/show/NCT00749827

Link

https://clinicaltrials.gov/show/NCT00749827

Keywords

Versions (1)
  1. 1/12/18 1/12/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

January 12, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Contrast Induced Nephropathy NCT00749827

English

Eligibility Contrast Induced Nephropathy NCT00749827

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
booked for cardiac angiography and/or percutaneous coronary intervention
Description

Angiocardiography Scheduled | Percutaneous Coronary Intervention Scheduled

Data type

boolean

Alias
UMLS CUI [1,1]
C0002971
UMLS CUI [1,2]
C0205539
UMLS CUI [2,1]
C1532338
UMLS CUI [2,2]
C0205539
pre-existing reduced kidney function (estimated gfr < 60 mls/min/1.73m2 by mdrd equation[18]).
Description

Decreased renal function Pre-existing | eGFR MDRD

Data type

boolean

Alias
UMLS CUI [1,1]
C0232807
UMLS CUI [1,2]
C2347662
UMLS CUI [2,1]
C3811844
UMLS CUI [2,2]
C3839656
minimum age 20 years
Description

Age Minimum

Data type

boolean

Alias
UMLS CUI [1,1]
C0001779
UMLS CUI [1,2]
C1524031
able to return to the study site for followup blood work.
Description

Patient Available Follow-up Hematologic Tests

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0470187
UMLS CUI [1,3]
C1522577
UMLS CUI [1,4]
C0018941
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
estimated gfr < 15 mls/min/1.73m2 by mdrd equation
Description

eGFR MDRD

Data type

boolean

Alias
UMLS CUI [1,1]
C3811844
UMLS CUI [1,2]
C3839656
already on dialysis
Description

Dialysis

Data type

boolean

Alias
UMLS CUI [1]
C0011946
known current acute kidney failure with serum creatinine rise of > 45 mol/l within 24 hours
Description

Kidney Failure | Serum creatinine raised

Data type

boolean

Alias
UMLS CUI [1]
C0035078
UMLS CUI [2]
C0700225
pulmonary edema - current or within 48 hours
Description

Pulmonary Edema

Data type

boolean

Alias
UMLS CUI [1]
C0034063
clinically significant ascites, edema or other fluid overload
Description

Ascites | Edema | Fluid overload

Data type

boolean

Alias
UMLS CUI [1]
C0003962
UMLS CUI [2]
C0013604
UMLS CUI [3]
C0546817
uncontrolled hypertension (> 165 mmhg systolic, or > 105 mmhg diastolic)
Description

Uncontrolled hypertension | Systolic Pressure | Diastolic blood pressure

Data type

boolean

Alias
UMLS CUI [1]
C1868885
UMLS CUI [2]
C0871470
UMLS CUI [3]
C0428883
unstable patient requiring iv nitroglycerine, or iv fluid or inotropes for bp support
Description

Patient Unstable status | Nitroglycerin Intravenous Blood Pressure Support | Intravenous fluid Blood Pressure Support | Inotropic agent Blood Pressure Support

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C0443343
UMLS CUI [2,1]
C0017887
UMLS CUI [2,2]
C1522726
UMLS CUI [2,3]
C0005823
UMLS CUI [2,4]
C1521721
UMLS CUI [3,1]
C1289919
UMLS CUI [3,2]
C0005823
UMLS CUI [3,3]
C1521721
UMLS CUI [4,1]
C0304509
UMLS CUI [4,2]
C0005823
UMLS CUI [4,3]
C1521721
emergency angiography
Description

Emergency Angiography

Data type

boolean

Alias
UMLS CUI [1,1]
C0013956
UMLS CUI [1,2]
C0002978
planned primary pci for acute coronary syndrome or myocardial infarction
Description

Percutaneous Coronary Intervention Primary Planned Acute Coronary Syndrome | Percutaneous Coronary Intervention Primary Planned Myocardial Infarction

Data type

boolean

Alias
UMLS CUI [1,1]
C1532338
UMLS CUI [1,2]
C0205225
UMLS CUI [1,3]
C1301732
UMLS CUI [1,4]
C0948089
UMLS CUI [2,1]
C1532338
UMLS CUI [2,2]
C0205225
UMLS CUI [2,3]
C1301732
UMLS CUI [2,4]
C0027051
exposure to iodinated radiocontrast within 3 days prior to study
Description

Exposure to Iodine containing radiocontrast media

Data type

boolean

Alias
UMLS CUI [1,1]
C0332157
UMLS CUI [1,2]
C0878652
prior anaphylactoid reaction to contrast
Description

Anaphylactoid reaction to radiocontrast media

Data type

boolean

Alias
UMLS CUI [1]
C1304190
planned administration of n-acetyl-cysteine, dopamine, fenoldopam or mannitol
Description

Acetylcysteine Planned | Dopamine Planned | Fenoldopam Planned | Mannitol Planned

Data type

boolean

Alias
UMLS CUI [1,1]
C0001047
UMLS CUI [1,2]
C1301732
UMLS CUI [2,1]
C0013030
UMLS CUI [2,2]
C1301732
UMLS CUI [3,1]
C0060180
UMLS CUI [3,2]
C1301732
UMLS CUI [4,1]
C0024730
UMLS CUI [4,2]
C1301732
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Similar models

Eligibility Contrast Induced Nephropathy NCT00749827

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Angiocardiography Scheduled | Percutaneous Coronary Intervention Scheduled
Item
booked for cardiac angiography and/or percutaneous coronary intervention
boolean
C0002971 (UMLS CUI [1,1])
C0205539 (UMLS CUI [1,2])
C1532338 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Decreased renal function Pre-existing | eGFR MDRD
Item
pre-existing reduced kidney function (estimated gfr < 60 mls/min/1.73m2 by mdrd equation[18]).
boolean
C0232807 (UMLS CUI [1,1])
C2347662 (UMLS CUI [1,2])
C3811844 (UMLS CUI [2,1])
C3839656 (UMLS CUI [2,2])
Age Minimum
Item
minimum age 20 years
boolean
C0001779 (UMLS CUI [1,1])
C1524031 (UMLS CUI [1,2])
Patient Available Follow-up Hematologic Tests
Item
able to return to the study site for followup blood work.
boolean
C0030705 (UMLS CUI [1,1])
C0470187 (UMLS CUI [1,2])
C1522577 (UMLS CUI [1,3])
C0018941 (UMLS CUI [1,4])
Item Group
C0680251 (UMLS CUI)
eGFR MDRD
Item
estimated gfr < 15 mls/min/1.73m2 by mdrd equation
boolean
C3811844 (UMLS CUI [1,1])
C3839656 (UMLS CUI [1,2])
Dialysis
Item
already on dialysis
boolean
C0011946 (UMLS CUI [1])
Kidney Failure | Serum creatinine raised
Item
known current acute kidney failure with serum creatinine rise of > 45 mol/l within 24 hours
boolean
C0035078 (UMLS CUI [1])
C0700225 (UMLS CUI [2])
Pulmonary Edema
Item
pulmonary edema - current or within 48 hours
boolean
C0034063 (UMLS CUI [1])
Ascites | Edema | Fluid overload
Item
clinically significant ascites, edema or other fluid overload
boolean
C0003962 (UMLS CUI [1])
C0013604 (UMLS CUI [2])
C0546817 (UMLS CUI [3])
Uncontrolled hypertension | Systolic Pressure | Diastolic blood pressure
Item
uncontrolled hypertension (> 165 mmhg systolic, or > 105 mmhg diastolic)
boolean
C1868885 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Patient Unstable status | Nitroglycerin Intravenous Blood Pressure Support | Intravenous fluid Blood Pressure Support | Inotropic agent Blood Pressure Support
Item
unstable patient requiring iv nitroglycerine, or iv fluid or inotropes for bp support
boolean
C0030705 (UMLS CUI [1,1])
C0443343 (UMLS CUI [1,2])
C0017887 (UMLS CUI [2,1])
C1522726 (UMLS CUI [2,2])
C0005823 (UMLS CUI [2,3])
C1521721 (UMLS CUI [2,4])
C1289919 (UMLS CUI [3,1])
C0005823 (UMLS CUI [3,2])
C1521721 (UMLS CUI [3,3])
C0304509 (UMLS CUI [4,1])
C0005823 (UMLS CUI [4,2])
C1521721 (UMLS CUI [4,3])
Emergency Angiography
Item
emergency angiography
boolean
C0013956 (UMLS CUI [1,1])
C0002978 (UMLS CUI [1,2])
Percutaneous Coronary Intervention Primary Planned Acute Coronary Syndrome | Percutaneous Coronary Intervention Primary Planned Myocardial Infarction
Item
planned primary pci for acute coronary syndrome or myocardial infarction
boolean
C1532338 (UMLS CUI [1,1])
C0205225 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
C0948089 (UMLS CUI [1,4])
C1532338 (UMLS CUI [2,1])
C0205225 (UMLS CUI [2,2])
C1301732 (UMLS CUI [2,3])
C0027051 (UMLS CUI [2,4])
Exposure to Iodine containing radiocontrast media
Item
exposure to iodinated radiocontrast within 3 days prior to study
boolean
C0332157 (UMLS CUI [1,1])
C0878652 (UMLS CUI [1,2])
Anaphylactoid reaction to radiocontrast media
Item
prior anaphylactoid reaction to contrast
boolean
C1304190 (UMLS CUI [1])
Acetylcysteine Planned | Dopamine Planned | Fenoldopam Planned | Mannitol Planned
Item
planned administration of n-acetyl-cysteine, dopamine, fenoldopam or mannitol
boolean
C0001047 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0013030 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C0060180 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
C0024730 (UMLS CUI [4,1])
C1301732 (UMLS CUI [4,2])
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