ID

29449

Description

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

Keywords

  1. 3/26/18 3/26/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

March 26, 2018

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Heart Failure NCT00549614

Eligibility Heart Failure NCT00549614

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
ef<40 %
Description

Cardiac ejection fraction

Data type

boolean

Alias
UMLS CUI [1]
C0232174
ihd
Description

Myocardial Ischemia

Data type

boolean

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

New York Heart Association Classification

Data type

boolean

Alias
UMLS CUI [1]
C1275491
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnancy
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
severe renal failure
Description

Kidney Failure Severe

Data type

boolean

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

Bradyarrhythmia | Tachyarrhythmia

Data type

boolean

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

Valvular Stenosis Severe

Data type

boolean

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

Myocardial Infarction

Data type

boolean

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

Insulin regime Diabetes Mellitus

Data type

boolean

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

Peptic Ulcer

Data type

boolean

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

Pregnancy | Breast Feeding

Data type

boolean

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

Hypersensitivity Investigational New Drugs

Data type

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)
Data type
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])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial