ID

17451

Beschreibung

Effect of NT-proBNP Guided Treatment of Chronic Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00149422

Link

https://clinicaltrials.gov/show/NCT00149422

Stichworte

  1. 15.09.16 15.09.16 -
Hochgeladen am

15. September 2016

DOI

Für eine Beantragung loggen Sie sich ein.

Lizenz

Creative Commons BY 4.0

Modell Kommentare :

Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.

Itemgroup Kommentare für :

Item Kommentare für :

Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.

Eligibility Heart Failure, Congestive NCT00149422

Eligibility Heart Failure, Congestive NCT00149422

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
admission because of congestive heart failure
Beschreibung

Congestive heart failure

Datentyp

boolean

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

NT-proBNP increased

Datentyp

boolean

Alias
UMLS CUI [1]
C3203735
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
life-threatening cardiac arrhythmias
Beschreibung

Cardiac Arrhythmia Life Threatening

Datentyp

boolean

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

Intervention Urgent

Datentyp

boolean

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

Lung disease Severe

Datentyp

boolean

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

Disease Life Threatening

Datentyp

boolean

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

Study Subject Participation Status | Informed Consent

Datentyp

boolean

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

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

Datentyp

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
Beschreibung

Informed Consent Unwilling

Datentyp

boolean

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

Hemodialysis | Peritoneal Dialysis, Continuous Ambulatory

Datentyp

boolean

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

Ähnliche Modelle

Eligibility Heart Failure, Congestive NCT00149422

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
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])

Benutzen Sie dieses Formular für Rückmeldungen, Fragen und Verbesserungsvorschläge.

Mit * gekennzeichnete Felder sind notwendig.

Benötigen Sie Hilfe bei der Suche? Um mehr Details zu erfahren und die Suche effektiver nutzen zu können schauen Sie sich doch das entsprechende Video auf unserer Tutorial Seite an.

Zum Video