Eligibility Heart Failure, Congestive NCT00149422

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
admission because of congestive heart failure
Beskrivning

Congestive heart failure

Datatyp

boolean

Alias
UMLS CUI [1]
C0018802
elevated nt-probnp levels on admission
Beskrivning

NT-proBNP increased

Datatyp

boolean

Alias
UMLS CUI [1]
C3203735
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
life-threatening cardiac arrhythmias
Beskrivning

Cardiac Arrhythmia Life Threatening

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0003811
UMLS CUI [1,2]
C2826244
urgent intervention
Beskrivning

Intervention Urgent

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1948041
UMLS CUI [1,2]
C0439609
severe lung disease
Beskrivning

Lung disease Severe

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0024115
UMLS CUI [1,2]
C0205082
presence of life threatening disease
Beskrivning

Disease Life Threatening

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2826244
signed informed consent for other study
Beskrivning

Study Subject Participation Status | Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0021430
mental or physical status not allowing written informed consent.
Beskrivning

Mental condition Excludes Informed Consent | patient physical state Excludes Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1,1]
C3840291
UMLS CUI [1,2]
C0332196
UMLS CUI [1,3]
C0021430
UMLS CUI [2,1]
C0679834
UMLS CUI [2,2]
C0332196
UMLS CUI [2,3]
C0021430
unwillingness to give informed consent
Beskrivning

Informed Consent Unwilling

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0558080
patients undergoing haemodialysis or continuous ambulatory peritoneal dialysis (capd)
Beskrivning

Hemodialysis | Peritoneal Dialysis, Continuous Ambulatory

Datatyp

boolean

Alias
UMLS CUI [1]
C0019004
UMLS CUI [2]
C0031140

Similar models

Eligibility Heart Failure, Congestive NCT00149422

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Congestive heart failure
Item
admission because of congestive heart failure
boolean
C0018802 (UMLS CUI [1])
NT-proBNP increased
Item
elevated nt-probnp levels on admission
boolean
C3203735 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Cardiac Arrhythmia Life Threatening
Item
life-threatening cardiac arrhythmias
boolean
C0003811 (UMLS CUI [1,1])
C2826244 (UMLS CUI [1,2])
Intervention Urgent
Item
urgent intervention
boolean
C1948041 (UMLS CUI [1,1])
C0439609 (UMLS CUI [1,2])
Lung disease Severe
Item
severe lung disease
boolean
C0024115 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Disease Life Threatening
Item
presence of life threatening disease
boolean
C0012634 (UMLS CUI [1,1])
C2826244 (UMLS CUI [1,2])
Study Subject Participation Status | Informed Consent
Item
signed informed consent for other study
boolean
C2348568 (UMLS CUI [1])
C0021430 (UMLS CUI [2])
Mental condition Excludes Informed Consent | patient physical state Excludes Informed Consent
Item
mental or physical status not allowing written informed consent.
boolean
C3840291 (UMLS CUI [1,1])
C0332196 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,3])
C0679834 (UMLS CUI [2,1])
C0332196 (UMLS CUI [2,2])
C0021430 (UMLS CUI [2,3])
Informed Consent Unwilling
Item
unwillingness to give informed consent
boolean
C0021430 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
Hemodialysis | Peritoneal Dialysis, Continuous Ambulatory
Item
patients undergoing haemodialysis or continuous ambulatory peritoneal dialysis (capd)
boolean
C0019004 (UMLS CUI [1])
C0031140 (UMLS CUI [2])