Eligibility Chronic Heart Failure NCT01794598

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
lvef ≤ 35%.
Description

lvef

Data type

boolean

Alias
UMLS CUI [1]
C0428772
nyha class ii, iii, or iv heart failure for the previous three months despite a minimum of 6 weeks of treatment.
Description

nyha

Data type

boolean

Alias
UMLS CUI [1]
C1275491
must be on optimal heart failure therapy according to aha/acc and hfsa heart failure guidelines, including treatment with acei and beta-blocker therapy, or have documented rationale for variation, including intolerance, contraindication, patient preference, or personal physician's judgment.
Description

heart failure therapy, beta blockers

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0018801
UMLS CUI [2]
C0001645
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
age less than 18.
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
currently pregnant or intending to become pregnant in the next year.
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
cardiovascular procedure or hospitalization for any reason planned in the next 6 months.
Description

cardiovascular procedure or hospitalization

Data type

boolean

Alias
UMLS CUI [1]
C0189573
UMLS CUI [2]
C0019993
expectation of receiving a cardiac transplant in the next six months.
Description

expected cardiac transplant

Data type

boolean

Alias
UMLS CUI [1,1]
C0018823
UMLS CUI [1,2]
C1517001
unable to provide the study consent.
Description

study consent

Data type

boolean

Alias
UMLS CUI [1]
C4034855
participation another clinical trial(s) that may interfere with follow-up or data collection for this study, or that may affect cardiovascular mortality.
Description

study participation

Data type

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Chronic Heart Failure NCT01794598

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Item Group
C1512693 (UMLS CUI)
lvef
Item
lvef ≤ 35%.
boolean
C0428772 (UMLS CUI [1])
nyha
Item
nyha class ii, iii, or iv heart failure for the previous three months despite a minimum of 6 weeks of treatment.
boolean
C1275491 (UMLS CUI [1])
heart failure therapy, beta blockers
Item
must be on optimal heart failure therapy according to aha/acc and hfsa heart failure guidelines, including treatment with acei and beta-blocker therapy, or have documented rationale for variation, including intolerance, contraindication, patient preference, or personal physician's judgment.
boolean
C0087111 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
C0001645 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
age
Item
age less than 18.
boolean
C0001779 (UMLS CUI [1])
Pregnancy
Item
currently pregnant or intending to become pregnant in the next year.
boolean
C0032961 (UMLS CUI [1])
cardiovascular procedure or hospitalization
Item
cardiovascular procedure or hospitalization for any reason planned in the next 6 months.
boolean
C0189573 (UMLS CUI [1])
C0019993 (UMLS CUI [2])
expected cardiac transplant
Item
expectation of receiving a cardiac transplant in the next six months.
boolean
C0018823 (UMLS CUI [1,1])
C1517001 (UMLS CUI [1,2])
study consent
Item
unable to provide the study consent.
boolean
C4034855 (UMLS CUI [1])
study participation
Item
participation another clinical trial(s) that may interfere with follow-up or data collection for this study, or that may affect cardiovascular mortality.
boolean
C2348568 (UMLS CUI [1])