ID

20508

Beschreibung

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

Link

https://clinicaltrials.gov/show/NCT00531765

Stichworte

  1. 28.02.17 28.02.17 -
Hochgeladen am

28. Februar 2017

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Contrast Induced Nephropathy NCT00531765

Eligibility Contrast Induced Nephropathy NCT00531765

Inclusion Criteria
Beschreibung

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
Beschreibung

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

Datentyp

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
Beschreibung

Exclusion Criteria

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

ID.2

Datentyp

boolean

acute renal failure
Beschreibung

acute renal failure

Datentyp

boolean

Alias
UMLS CUI [1]
C0022660
cardiogenic shock
Beschreibung

cardiogenic shock

Datentyp

boolean

Alias
UMLS CUI [1]
C0036980
emergency cardiac catheterization
Beschreibung

emergency cardiac catheterization

Datentyp

boolean

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

preexisting peritoneal or hemodialysis

Datentyp

boolean

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

pregnancy

Datentyp

boolean

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

Contrast Media; exposure history

Datentyp

boolean

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

allergy to contrast

Datentyp

boolean

Alias
UMLS CUI [1]
C0570562
renal transplant,
Beschreibung

renal transplant

Datentyp

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
Beschreibung

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

Datentyp

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
Beschreibung

pulmonary edema, congestive heart failure

Datentyp

boolean

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

n-acetylcystein

Datentyp

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).
Beschreibung

nsaids

Datentyp

boolean

Alias
UMLS CUI [1]
C0003211

Ähnliche Modelle

Eligibility Contrast Induced Nephropathy NCT00531765

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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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