ID

20508

Beschrijving

Sodium Bicarbonate in Preventing Contrast Induced Nephropathy; ODM derived from: https://clinicaltrials.gov/show/NCT00531765

Link

https://clinicaltrials.gov/show/NCT00531765

Trefwoorden

  1. 28-02-17 28-02-17 -
Geüploaded op

28 februari 2017

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Contrast Induced Nephropathy NCT00531765

Eligibility Contrast Induced Nephropathy NCT00531765

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
all adult patients (18 years and above) who are scheduled for cardiac catechization and have abnormal but stable renal function will be eligible for enrollment. abnormal renal function is defined as a creatinine level exceeding the normal range (more than 115 or 96 um/l in males and females, respectively, in kfsh&rc laboratories) or egfr less than 60 ml/min
Beschrijving

Age | Percutaneous Coronary Intervention | Abnormal renal function; Glomerular Filtration Rate; Creatinine measurement, serum (procedure)

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C1532338
UMLS CUI [3,1]
C0151746
UMLS CUI [3,2]
C0017654
UMLS CUI [3,3]
C0201976
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who fall under any of the following categories will be excluded:
Beschrijving

ID.2

Datatype

boolean

acute renal failure
Beschrijving

acute renal failure

Datatype

boolean

Alias
UMLS CUI [1]
C0022660
cardiogenic shock
Beschrijving

cardiogenic shock

Datatype

boolean

Alias
UMLS CUI [1]
C0036980
emergency cardiac catheterization
Beschrijving

emergency cardiac catheterization

Datatype

boolean

Alias
UMLS CUI [1]
C1532297
preexisting peritoneal or hemodialysis
Beschrijving

preexisting peritoneal or hemodialysis

Datatype

boolean

Alias
UMLS CUI [1]
C0031139
UMLS CUI [2]
C0019004
pregnancy
Beschrijving

pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
recent exposure to contrast agent within the last 3 days
Beschrijving

Contrast Media; exposure history

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009924
UMLS CUI [1,2]
C2220266
allergy to contrast or any of the above treatment
Beschrijving

allergy to contrast

Datatype

boolean

Alias
UMLS CUI [1]
C0570562
renal transplant,
Beschrijving

renal transplant

Datatype

boolean

Alias
UMLS CUI [1]
C0022671
patients who received dopamine, mannitol, theophyllin or other medications known to affect renal function within one week from cardiac cath
Beschrijving

Prior Therapy; Dopamine; Mannitol; Theophylline | Adverse reaction to drug; Renal function

Datatype

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C0013030
UMLS CUI [1,3]
C0024730
UMLS CUI [1,4]
C0039771
UMLS CUI [2,1]
C0041755
UMLS CUI [2,2]
C0232804
pulmonary edema / congestive heart failure
Beschrijving

pulmonary edema, congestive heart failure

Datatype

boolean

Alias
UMLS CUI [1]
C0034063
UMLS CUI [2]
C0018802
use of n-acetylcystein
Beschrijving

n-acetylcystein

Datatype

boolean

Alias
UMLS CUI [1]
C0001047
patents on nsaids who can not stop using them for 48 hrs before and 48 hrs after procedure (except aspirin).
Beschrijving

nsaids

Datatype

boolean

Alias
UMLS CUI [1]
C0003211

Similar models

Eligibility Contrast Induced Nephropathy NCT00531765

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age | Percutaneous Coronary Intervention | Abnormal renal function; Glomerular Filtration Rate; Creatinine measurement, serum (procedure)
Item
all adult patients (18 years and above) who are scheduled for cardiac catechization and have abnormal but stable renal function will be eligible for enrollment. abnormal renal function is defined as a creatinine level exceeding the normal range (more than 115 or 96 um/l in males and females, respectively, in kfsh&rc laboratories) or egfr less than 60 ml/min
boolean
C0001779 (UMLS CUI [1])
C1532338 (UMLS CUI [2])
C0151746 (UMLS CUI [3,1])
C0017654 (UMLS CUI [3,2])
C0201976 (UMLS CUI [3,3])
Item Group
C0680251 (UMLS CUI)
ID.2
Item
patients who fall under any of the following categories will be excluded:
boolean
acute renal failure
Item
acute renal failure
boolean
C0022660 (UMLS CUI [1])
cardiogenic shock
Item
cardiogenic shock
boolean
C0036980 (UMLS CUI [1])
emergency cardiac catheterization
Item
emergency cardiac catheterization
boolean
C1532297 (UMLS CUI [1])
preexisting peritoneal or hemodialysis
Item
preexisting peritoneal or hemodialysis
boolean
C0031139 (UMLS CUI [1])
C0019004 (UMLS CUI [2])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Contrast Media; exposure history
Item
recent exposure to contrast agent within the last 3 days
boolean
C0009924 (UMLS CUI [1,1])
C2220266 (UMLS CUI [1,2])
allergy to contrast
Item
allergy to contrast or any of the above treatment
boolean
C0570562 (UMLS CUI [1])
renal transplant
Item
renal transplant,
boolean
C0022671 (UMLS CUI [1])
Prior Therapy; Dopamine; Mannitol; Theophylline | Adverse reaction to drug; Renal function
Item
patients who received dopamine, mannitol, theophyllin or other medications known to affect renal function within one week from cardiac cath
boolean
C1514463 (UMLS CUI [1,1])
C0013030 (UMLS CUI [1,2])
C0024730 (UMLS CUI [1,3])
C0039771 (UMLS CUI [1,4])
C0041755 (UMLS CUI [2,1])
C0232804 (UMLS CUI [2,2])
pulmonary edema, congestive heart failure
Item
pulmonary edema / congestive heart failure
boolean
C0034063 (UMLS CUI [1])
C0018802 (UMLS CUI [2])
n-acetylcystein
Item
use of n-acetylcystein
boolean
C0001047 (UMLS CUI [1])
nsaids
Item
patents on nsaids who can not stop using them for 48 hrs before and 48 hrs after procedure (except aspirin).
boolean
C0003211 (UMLS CUI [1])

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