Eligibility Heart Failure NCT01598740

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
heart failure with new york heart association (nyha) classification ii or iii
Beschreibung

ID.1

Datentyp

boolean

chronic kidney disease
Beschreibung

ID.2

Datentyp

boolean

cardiac ejection fraction <40%
Beschreibung

ID.3

Datentyp

boolean

on heart failure therapy including an acei or arb, and a bb
Beschreibung

ID.4

Datentyp

boolean

willing to understand and comply with study procedures and provide written informed consent.
Beschreibung

ID.5

Datentyp

boolean

Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
hospitalization within 4 weeks of baseline visit
Beschreibung

ID.6

Datentyp

boolean

history or presence of gastrointestinal conditions such as severe constipation or gastrointestinal tract strictures
Beschreibung

ID.7

Datentyp

boolean

current or anticipated dialysis during study
Beschreibung

ID.8

Datentyp

boolean

in the investigator's judgment, any cardiovascular, renal, hepatic, endocrine, gastrointestinal, neurological, or other disease or condition that makes the subject's study participation unsafe
Beschreibung

ID.9

Datentyp

boolean

drug or alcohol abuse
Beschreibung

ID.10

Datentyp

boolean

Ähnliche Modelle

Eligibility Heart Failure NCT01598740

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
heart failure with new york heart association (nyha) classification ii or iii
boolean
ID.2
Item
chronic kidney disease
boolean
ID.3
Item
cardiac ejection fraction <40%
boolean
ID.4
Item
on heart failure therapy including an acei or arb, and a bb
boolean
ID.5
Item
willing to understand and comply with study procedures and provide written informed consent.
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
hospitalization within 4 weeks of baseline visit
boolean
ID.7
Item
history or presence of gastrointestinal conditions such as severe constipation or gastrointestinal tract strictures
boolean
ID.8
Item
current or anticipated dialysis during study
boolean
ID.9
Item
in the investigator's judgment, any cardiovascular, renal, hepatic, endocrine, gastrointestinal, neurological, or other disease or condition that makes the subject's study participation unsafe
boolean
ID.10
Item
drug or alcohol abuse
boolean