Eligibility End Stage Renal Disease (ESRD) NCT01343251

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
esrd patients requiring hemodialysis
Beschreibung

ID.1

Datentyp

boolean

age > 18 years old
Beschreibung

ID.2

Datentyp

boolean

able to give informed consent
Beschreibung

ID.3

Datentyp

boolean

able to participate in quality of life survey
Beschreibung

ID.4

Datentyp

boolean

all patients who are not candidate for avf or avg
Beschreibung

ID.5

Datentyp

boolean

life expectancy 2 years or greater
Beschreibung

ID.6

Datentyp

boolean

willing and able to participate with follow-up examinations
Beschreibung

ID.7

Datentyp

boolean

Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or breastfeeding females
Beschreibung

ID.8

Datentyp

boolean

disorder that compromises the ability to give informed consent and/or comply with the study procedures
Beschreibung

ID.9

Datentyp

boolean

any medical condition that in the opinion of the investigator may pose a safety risk to a subject in the study or which may interfere with the study participation
Beschreibung

ID.10

Datentyp

boolean

Ähnliche Modelle

Eligibility End Stage Renal Disease (ESRD) NCT01343251

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
esrd patients requiring hemodialysis
boolean
ID.2
Item
age > 18 years old
boolean
ID.3
Item
able to give informed consent
boolean
ID.4
Item
able to participate in quality of life survey
boolean
ID.5
Item
all patients who are not candidate for avf or avg
boolean
ID.6
Item
life expectancy 2 years or greater
boolean
ID.7
Item
willing and able to participate with follow-up examinations
boolean
Item Group
C0680251 (UMLS CUI)
ID.8
Item
pregnant or breastfeeding females
boolean
ID.9
Item
disorder that compromises the ability to give informed consent and/or comply with the study procedures
boolean
ID.10
Item
any medical condition that in the opinion of the investigator may pose a safety risk to a subject in the study or which may interfere with the study participation
boolean