Informationen:
Fehler:
ID
22882
Beschreibung
Influence of Home Monitoring on the Clinical Status of Heart Failure Patients With an Impaired Left Ventricular Function; ODM derived from: https://clinicaltrials.gov/show/NCT00538356
Link
https://clinicaltrials.gov/show/NCT00538356
Stichworte
Versionen (1)
- 13.06.17 13.06.17 -
Hochgeladen am
13. Juni 2017
DOI
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Lizenz
Creative Commons BY 4.0
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Eligibility Ventricular Fibrillation NCT00538356
Eligibility Ventricular Fibrillation NCT00538356
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Ventricular Fibrillation NCT00538356
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
indication for single chamber icd, dual chamber icd or crt-d
Item
indication for single chamber icd, dual chamber icd or crt-d
boolean
C3146298 (UMLS CUI [1,1])
C2048118 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C2048117 (UMLS CUI [2,2])
C3146298 (UMLS CUI [3,1])
C1135480 (UMLS CUI [3,2])
C2048118 (UMLS CUI [1,2])
C3146298 (UMLS CUI [2,1])
C2048117 (UMLS CUI [2,2])
C3146298 (UMLS CUI [3,1])
C1135480 (UMLS CUI [3,2])
chronic heart failure
Item
chronic heart failure (≥ 3 months)
boolean
C0264716 (UMLS CUI [1])
nyha class
Item
nyha class ii or iii for 1 month prior to screening
boolean
C1882083 (UMLS CUI [1])
lvef
Item
lvef ≤ 35% within 3 months prior to screening
boolean
C0428772 (UMLS CUI [1])
indication for therapy with diuretics
Item
indication for therapy with diuretics
boolean
C0012798 (UMLS CUI [1,1])
C3146298 (UMLS CUI [1,2])
C3146298 (UMLS CUI [1,2])
informed consent
Item
patient informed consent
boolean
C0021430 (UMLS CUI [1])
uncontrolled hypertension
Item
uncontrolled hypertension
boolean
C1868885 (UMLS CUI [1])
nyha class
Item
nyha class i or iv
boolean
C1882083 (UMLS CUI [1])
permanent atrial fibrillation
Item
permanent atrial fibrillation
boolean
C2586056 (UMLS CUI [1])
life expectancy
Item
life expectancy < 1 year
boolean
C0023671 (UMLS CUI [1])
restrictive, infiltrative or hypertrophic cardiomyopathy, constrictive pericarditis, acute myocarditis
Item
restrictive, infiltrative or hypertrophic cardiomyopathy, constrictive pericarditis, acute myocarditis
boolean
C0007196 (UMLS CUI [1])
C0264839 (UMLS CUI [2])
C0007194 (UMLS CUI [3])
C0031048 (UMLS CUI [4])
C0155686 (UMLS CUI [5])
C0264839 (UMLS CUI [2])
C0007194 (UMLS CUI [3])
C0031048 (UMLS CUI [4])
C0155686 (UMLS CUI [5])
severe mitral regurgitation
Item
severe mitral regurgitation
boolean
C0026266 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,2])
symptomatic aortic stenosis
Item
symptomatic aortic stenosis
boolean
C0003507 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
C0231220 (UMLS CUI [1,2])
tricuspid valve replacement
Item
tricuspid valve replacement
boolean
C0190119 (UMLS CUI [1])
substance use disorder
Item
known drug or alcohol abuse
boolean
C0038586 (UMLS CUI [1])
compliance
Item
expected non-compliance
boolean
C1321605 (UMLS CUI [1])
pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
study subject participation status, telemonitoring
Item
participation in another telemonitoring concept
boolean
C2348568 (UMLS CUI [1,1])
C3898905 (UMLS CUI [1,2])
C3898905 (UMLS CUI [1,2])
participation in another study
Item
participation in another study
boolean
C2348568 (UMLS CUI [1])