Informatie:
Fout:
ID
28029
Beschrijving
Clinical Phenotyping Resource and Biobank Core of the Michigan O'Brien Renal Center; ODM derived from: https://clinicaltrials.gov/show/NCT01016613
Link
https://clinicaltrials.gov/show/NCT01016613
Trefwoorden
Versies (1)
- 11-12-17 11-12-17 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
11 december 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 Chronic Kidney Disease NCT01016613
Eligibility Chronic Kidney Disease NCT01016613
- StudyEvent: Eligibility
Similar models
Eligibility Chronic Kidney Disease NCT01016613
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age | Chronic Kidney Disease | Proteinuria | Decreased renal function Hematologic Tests
Item
persons of any age who have chronic kidney disease (abnormally high protein in urine or reduced kidney function determined by blood tests)
boolean
C0001779 (UMLS CUI [1])
C1561643 (UMLS CUI [2])
C0033687 (UMLS CUI [3])
C0232807 (UMLS CUI [4,1])
C0018941 (UMLS CUI [4,2])
C1561643 (UMLS CUI [2])
C0033687 (UMLS CUI [3])
C0232807 (UMLS CUI [4,1])
C0018941 (UMLS CUI [4,2])
Patients Few Chronic Kidney Disease Absence
Item
a small number of people without chronic kidney disease
boolean
C0030705 (UMLS CUI [1,1])
C0205388 (UMLS CUI [1,2])
C1561643 (UMLS CUI [1,3])
C0332197 (UMLS CUI [1,4])
C0205388 (UMLS CUI [1,2])
C1561643 (UMLS CUI [1,3])
C0332197 (UMLS CUI [1,4])
Hemodialysis | Peritoneal Dialysis
Item
people on hemodialysis or peritoneal dialysis
boolean
C0019004 (UMLS CUI [1])
C0031139 (UMLS CUI [2])
C0031139 (UMLS CUI [2])
Kidney Transplantation
Item
people who have had a kidney transplant
boolean
C0022671 (UMLS CUI [1])
Informed Consent Unable | Informed Consent Unwilling
Item
people unable or unwilling to provide consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
women who are pregnant or nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Polycystic Kidney Disease
Item
people who have polycystic kidney disease
boolean
C0022680 (UMLS CUI [1])
Hemoglobin measurement
Item
people with a hemoglobin of <9 at the time of enrollment
boolean
C0518015 (UMLS CUI [1])
Institutionalized Persons
Item
institutionalized persons
boolean
C0376326 (UMLS CUI [1])
Study Subject Participation Status | Blinded Clinical Study Interventional
Item
people currently participating in a blinded interventional clinical trial
boolean
C2348568 (UMLS CUI [1])
C2347038 (UMLS CUI [2,1])
C0184661 (UMLS CUI [2,2])
C2347038 (UMLS CUI [2,1])
C0184661 (UMLS CUI [2,2])