Informações:
Falhas:
ID
26199
Descrição
Omega-3-Polyunsaturated Fatty-Acids (N3-Pufa) In Patients With Severe Chronic Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00149409
Link
https://clinicaltrials.gov/show/NCT00149409
Palavras-chave
Versões (1)
- 11/10/2017 11/10/2017 -
Titular dos direitos
see clinicaltrials.gov
Transferido a
11 de outubro de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Chronic Heart Failure NCT00149409
Eligibility Chronic Heart Failure NCT00149409
- StudyEvent: Eligibility
Similar models
Eligibility Chronic Heart Failure NCT00149409
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
non ischemic chronic heart failure
Item
chronic heart failure of non-ischemic origin
boolean
C0018801 (UMLS CUI [1,1])
C0475224 (UMLS CUI [1,2])
C1518422 (UMLS CUI [1,3])
C0475224 (UMLS CUI [1,2])
C1518422 (UMLS CUI [1,3])
Age
Item
Age
integer
C0001779 (UMLS CUI [1])
NYHA functional class iii-iv
Item
nyha functional class iii-iv
boolean
C0278962 (UMLS CUI [1])
Left ventricular ejection fraction
Item
lvef < 35 %
boolean
C0428772 (UMLS CUI [1])
Heart failure therapy
Item
optimized heart failure therapy
boolean
C0087111 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,2])
Brain natriuretic peptide measurement
Item
plasma nt-bnp >2000pg/ml
boolean
C1095989 (UMLS CUI [1])
Treatment with omacor or other fish oil products
Item
current treatment with omacor or other fish oil products
boolean
C2826666 (UMLS CUI [1,1])
C0912903 (UMLS CUI [1,2])
C2826666 (UMLS CUI [2,1])
C0016157 (UMLS CUI [2,2])
C0912903 (UMLS CUI [1,2])
C2826666 (UMLS CUI [2,1])
C0016157 (UMLS CUI [2,2])
Hypersensitivity to study drug
Item
known hypersensitivity to the study drug
boolean
C0020517 (UMLS CUI [1,1])
C0304229 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,2])
Ischemic cardiomyopathy
Item
ischemic cardiomyopathy
boolean
C0349782 (UMLS CUI [1])
Uncorrected significant valvular heart disease
Item
uncorrected significant valvular heart disease
boolean
C0018824 (UMLS CUI [1,1])
C0750502 (UMLS CUI [1,2])
C0750502 (UMLS CUI [1,2])
Heart failure due to congenital heart disease
Item
heart failure due to congenital heart disease
boolean
C0018801 (UMLS CUI [1,1])
C0152021 (UMLS CUI [1,2])
C0152021 (UMLS CUI [1,2])
Restrictive cardiomyopathy
Item
restrictive cardiomyopathy
boolean
C0007196 (UMLS CUI [1])
Alcohol related heart disease
Item
alcoholic heart disease
boolean
C0018799 (UMLS CUI [1,1])
C0236664 (UMLS CUI [1,2])
C0236664 (UMLS CUI [1,2])
Acute myocarditis
Item
acute myocarditis
boolean
C0155686 (UMLS CUI [1])
Continuos intravenous therapy
Item
continuous i.v. therapy for heart failure
boolean
C1411942 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
C0549178 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
Heart-Assist Devices
Item
mechanical assist device
boolean
C0018831 (UMLS CUI [1])
Life expectancy limited Comorbidity
Item
life expectancy <1 year due to non-cardiac causes
boolean
C0023671 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
Ability to perform bicycle testing
Item
inability to perform bicycle testing
boolean
C0005376 (UMLS CUI [1,1])
C0085732 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,2])
Childbearing Potential and contraceptive methods
Item
women of childbearing potential not practicing a save contraception method
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0700589 (UMLS CUI [1,2])
Study Subject Participation Status
Item
current participation in another intervention study
boolean
C2348568 (UMLS CUI [1,1])
C3274035 (UMLS CUI [1,2])
C3274035 (UMLS CUI [1,2])
Participation in another interventional study within the last 3 months
Item
participation in another study with an intervention within the last 3 months.
boolean
C2348568 (UMLS CUI [1,1])
C3274035 (UMLS CUI [1,2])
C4086725 (UMLS CUI [1,3])
C3274035 (UMLS CUI [1,2])
C4086725 (UMLS CUI [1,3])