ID

29449

Beschrijving

Effect of 4 Weeks Treatment With Acipimox in Patients With Chronic Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00549614

Link

https://clinicaltrials.gov/show/NCT00549614

Trefwoorden

  1. 26-03-18 26-03-18 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

26 maart 2018

DOI

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Licentie

Creative Commons BY 4.0

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Eligibility Heart Failure NCT00549614

Eligibility Heart Failure NCT00549614

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
ef<40 %
Beschrijving

Cardiac ejection fraction

Datatype

boolean

Alias
UMLS CUI [1]
C0232174
ihd
Beschrijving

Myocardial Ischemia

Datatype

boolean

Alias
UMLS CUI [1]
C0151744
nyha-class ii-iii.
Beschrijving

New York Heart Association Classification

Datatype

boolean

Alias
UMLS CUI [1]
C1275491
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy
Beschrijving

Pregnancy

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
severe renal failure
Beschrijving

Kidney Failure Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C0035078
UMLS CUI [1,2]
C0205082
new brady- or tachyarrhythmia
Beschrijving

Bradyarrhythmia | Tachyarrhythmia

Datatype

boolean

Alias
UMLS CUI [1]
C0079035
UMLS CUI [2]
C0080203
severe stenotic valvular disease
Beschrijving

Valvular Stenosis Severe

Datatype

boolean

Alias
UMLS CUI [1,1]
C1883524
UMLS CUI [1,2]
C0205082
myocardial infarction within last 6 weeks
Beschrijving

Myocardial Infarction

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
insulin treated diabetes mellitus
Beschrijving

Insulin regime Diabetes Mellitus

Datatype

boolean

Alias
UMLS CUI [1,1]
C0557978
UMLS CUI [1,2]
C0011849
peptic ulcer
Beschrijving

Peptic Ulcer

Datatype

boolean

Alias
UMLS CUI [1]
C0030920
pregnancy or lactating women
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
allergy towards tested medicine
Beschrijving

Hypersensitivity Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0013230

Similar models

Eligibility Heart Failure NCT00549614

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Cardiac ejection fraction
Item
ef<40 %
boolean
C0232174 (UMLS CUI [1])
Myocardial Ischemia
Item
ihd
boolean
C0151744 (UMLS CUI [1])
New York Heart Association Classification
Item
nyha-class ii-iii.
boolean
C1275491 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Kidney Failure Severe
Item
severe renal failure
boolean
C0035078 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Bradyarrhythmia | Tachyarrhythmia
Item
new brady- or tachyarrhythmia
boolean
C0079035 (UMLS CUI [1])
C0080203 (UMLS CUI [2])
Valvular Stenosis Severe
Item
severe stenotic valvular disease
boolean
C1883524 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Myocardial Infarction
Item
myocardial infarction within last 6 weeks
boolean
C0027051 (UMLS CUI [1])
Insulin regime Diabetes Mellitus
Item
insulin treated diabetes mellitus
boolean
C0557978 (UMLS CUI [1,1])
C0011849 (UMLS CUI [1,2])
Peptic Ulcer
Item
peptic ulcer
boolean
C0030920 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnancy or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Hypersensitivity Investigational New Drugs
Item
allergy towards tested medicine
boolean
C0020517 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])

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