Informatie:
Fout:
ID
20261
Beschrijving
Prevention of Contrast Induced Nephropathy With Sodium Bicarbonate; ODM derived from: https://clinicaltrials.gov/show/NCT00392405
Link
https://clinicaltrials.gov/show/NCT00392405
Trefwoorden
Versies (1)
- 17-02-17 17-02-17 -
Geüploaded op
17 februari 2017
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Contrast Induced Nephropathy NCT00392405
Eligibility Contrast Induced Nephropathy NCT00392405
- StudyEvent: Eligibility
Similar models
Eligibility Contrast Induced Nephropathy NCT00392405
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
C0742919 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Age
Item
18+ years of age
boolean
C0001779 (UMLS CUI [1])
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])
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])
C0392747 (UMLS CUI [1,2])
Dialysis Pre-existing
Item
pre-existing dialysis patient
boolean
C0011946 (UMLS CUI [1,1])
C2347662 (UMLS CUI [1,2])
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])
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])
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])
C0060180 (UMLS CUI [2])
C0024730 (UMLS CUI [3])
C0699252 (UMLS CUI [4])
Myocardial Infarction
Item
acute myocardial infarction
boolean
C0027051 (UMLS CUI [1])