ID

20261

Descripción

Prevention of Contrast Induced Nephropathy With Sodium Bicarbonate; ODM derived from: https://clinicaltrials.gov/show/NCT00392405

Link

https://clinicaltrials.gov/show/NCT00392405

Palabras clave

Versiones (1)
  1. 17/2/17 17/2/17 -
Subido en

17 de febrero de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Contrast Induced Nephropathy NCT00392405

Inglés

Eligibility Contrast Induced Nephropathy NCT00392405

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
stage iii chronic kidney disease (gfr 30-60ml/min per 1.73m2 calculated by using mdrd equation)
Descripción

Chronic Kidney Disease stage | Renal function GFR estimation by MDRD

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1561643
UMLS CUI [1,2]
C0699749
UMLS CUI [2]
C2170215
inpatients at norton community hospital scheduled to undergo diagnostic ct scan using contrast between the hours of 7am and 6pm
Descripción

inpatient | CT scan contrast Scheduled

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021562
UMLS CUI [2,1]
C0742919
UMLS CUI [2,2]
C0205539
18+ years of age
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
exclusion criteria
Descripción

ID.4

Tipo de datos

boolean

current clinical diagnosis of exacerbated congestive heart failure
Descripción

Congestive heart failure Exacerbated

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0018802
UMLS CUI [1,2]
C1444749
creatinine >8 mg/dl
Descripción

Creatinine measurement, serum

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201976
change in serum cre of at least 0.5mg/dl during previous 24hours
Descripción

Serum creatinine level Change

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0600061
UMLS CUI [1,2]
C0392747
pre-existing dialysis patient
Descripción

Dialysis Pre-existing

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0011946
UMLS CUI [1,2]
C2347662
multiple myeloma
Descripción

Multiple Myeloma

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0026764
uncontrolled hypertension (definition: treated sbp >160mmhg or dbp >100mmhg
Descripción

Uncontrolled hypertension | Systolic Pressure Treated | Diastolic blood pressure Treated

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1868885
UMLS CUI [2,1]
C0871470
UMLS CUI [2,2]
C1522326
UMLS CUI [3,1]
C0428883
UMLS CUI [3,2]
C1522326
exposure to contrast 48 hours prior to study
Descripción

Contrast Media Exposure to

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009924
UMLS CUI [1,2]
C0332157
allergy to contrast dye
Descripción

contrast dye allergy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0742797
pregnancy
Descripción

Pregnancy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032961
patient has received pressor agents, fendolapam, mannitol, or mucomyst at time of study
Descripción

Pressors | Fenoldopam | Mannitol | Mucomyst

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0237795
UMLS CUI [2]
C0060180
UMLS CUI [3]
C0024730
UMLS CUI [4]
C0699252
acute myocardial infarction
Descripción

Myocardial Infarction

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
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Similar models

Eligibility Contrast Induced Nephropathy NCT00392405

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Chronic Kidney Disease stage | Renal function GFR estimation by MDRD
Item
stage iii chronic kidney disease (gfr 30-60ml/min per 1.73m2 calculated by using mdrd equation)
boolean
C1561643 (UMLS CUI [1,1])
C0699749 (UMLS CUI [1,2])
C2170215 (UMLS CUI [2])
inpatient | CT scan contrast Scheduled
Item
inpatients at norton community hospital scheduled to undergo diagnostic ct scan using contrast between the hours of 7am and 6pm
boolean
C0021562 (UMLS CUI [1])
C0742919 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Age
Item
18+ years of age
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
ID.4
Item
exclusion criteria
boolean
Congestive heart failure Exacerbated
Item
current clinical diagnosis of exacerbated congestive heart failure
boolean
C0018802 (UMLS CUI [1,1])
C1444749 (UMLS CUI [1,2])
Creatinine measurement, serum
Item
creatinine >8 mg/dl
boolean
C0201976 (UMLS CUI [1])
Serum creatinine level Change
Item
change in serum cre of at least 0.5mg/dl during previous 24hours
boolean
C0600061 (UMLS CUI [1,1])
C0392747 (UMLS CUI [1,2])
Dialysis Pre-existing
Item
pre-existing dialysis patient
boolean
C0011946 (UMLS CUI [1,1])
C2347662 (UMLS CUI [1,2])
Multiple Myeloma
Item
multiple myeloma
boolean
C0026764 (UMLS CUI [1])
Uncontrolled hypertension | Systolic Pressure Treated | Diastolic blood pressure Treated
Item
uncontrolled hypertension (definition: treated sbp >160mmhg or dbp >100mmhg
boolean
C1868885 (UMLS CUI [1])
C0871470 (UMLS CUI [2,1])
C1522326 (UMLS CUI [2,2])
C0428883 (UMLS CUI [3,1])
C1522326 (UMLS CUI [3,2])
Contrast Media Exposure to
Item
exposure to contrast 48 hours prior to study
boolean
C0009924 (UMLS CUI [1,1])
C0332157 (UMLS CUI [1,2])
contrast dye allergy
Item
allergy to contrast dye
boolean
C0742797 (UMLS CUI [1])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Pressors | Fenoldopam | Mannitol | Mucomyst
Item
patient has received pressor agents, fendolapam, mannitol, or mucomyst at time of study
boolean
C0237795 (UMLS CUI [1])
C0060180 (UMLS CUI [2])
C0024730 (UMLS CUI [3])
C0699252 (UMLS CUI [4])
Myocardial Infarction
Item
acute myocardial infarction
boolean
C0027051 (UMLS CUI [1])
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