ID

16829

Beschrijving

Oxypurinol Compared With Placebo for Class III-IV NYHA Congestive Heart Failure; ODM derived from: https://clinicaltrials.gov/show/NCT00063687

Link

https://clinicaltrials.gov/show/NCT00063687

Trefwoorden

Versies (1)
  1. 09-08-16 09-08-16 -
Geüploaded op

9 augustus 2016

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Congestive Heart Failure NCT00063687

Engels

Eligibility Congestive Heart Failure NCT00063687

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
18-85 years old,
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
stable nyha class iii-iv
Beschrijving

New York Heart Association Classification

Datatype

boolean

Alias
UMLS CUI [1]
C1275491
hospitalization or er visits in past 18 months for worsening heart failure (or addition of new heart failure medication added to regimen due to lack of stability on current regimen.
Beschrijving

Hospitalization Heart failure Worsening | Emergency room admission Heart failure Worsening | Therapeutic procedure Stable status Lack | Heart failure Pharmaceutical Preparation New

Datatype

boolean

Alias
UMLS CUI [1,1]
C0019993
UMLS CUI [1,2]
C0018801
UMLS CUI [1,3]
C0332271
UMLS CUI [2,1]
C0583237
UMLS CUI [2,2]
C0018801
UMLS CUI [2,3]
C0332271
UMLS CUI [3,1]
C0087111
UMLS CUI [3,2]
C0205360
UMLS CUI [3,3]
C0332268
UMLS CUI [4,1]
C0018801
UMLS CUI [4,2]
C0013227
UMLS CUI [4,3]
C0205314
ef =< 40%
Beschrijving

Cardiac ejection fraction

Datatype

boolean

Alias
UMLS CUI [1]
C0232174
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
any condition (other than chf) that could limit exercise
Beschrijving

Condition Limiting Exercise | Congestive heart failure

Datatype

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0015259
UMLS CUI [2]
C0018802
any concurrent disease likely to limit life expectancy.
Beschrijving

Comorbidity Probably Limiting Life Expectancy

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0750492
UMLS CUI [1,3]
C0439801
UMLS CUI [1,4]
C0023671
participation in another clinical trial
Beschrijving

Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1]
C2348568
primary valvular disease, active myocarditis, or an obstructive or restrictive cardio-myopathy
Beschrijving

primary valvular heart disease | Myocarditis | Hypertrophic Cardiomyopathy | Restrictive cardiomyopathy

Datatype

boolean

Alias
UMLS CUI [1]
C2064629
UMLS CUI [2]
C0027059
UMLS CUI [3]
C0007194
UMLS CUI [4]
C0007196
heart attack, stroke, unstable angina or cardiac surgery within previous 3 months
Beschrijving

Myocardial Infarction | Cerebrovascular accident | Angina, Unstable | Cardiac Surgery procedures

Datatype

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0038454
UMLS CUI [3]
C0002965
UMLS CUI [4]
C0018821
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Similar models

Eligibility Congestive Heart Failure NCT00063687

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
18-85 years old,
boolean
C0001779 (UMLS CUI [1])
New York Heart Association Classification
Item
stable nyha class iii-iv
boolean
C1275491 (UMLS CUI [1])
Hospitalization Heart failure Worsening | Emergency room admission Heart failure Worsening | Therapeutic procedure Stable status Lack | Heart failure Pharmaceutical Preparation New
Item
hospitalization or er visits in past 18 months for worsening heart failure (or addition of new heart failure medication added to regimen due to lack of stability on current regimen.
boolean
C0019993 (UMLS CUI [1,1])
C0018801 (UMLS CUI [1,2])
C0332271 (UMLS CUI [1,3])
C0583237 (UMLS CUI [2,1])
C0018801 (UMLS CUI [2,2])
C0332271 (UMLS CUI [2,3])
C0087111 (UMLS CUI [3,1])
C0205360 (UMLS CUI [3,2])
C0332268 (UMLS CUI [3,3])
C0018801 (UMLS CUI [4,1])
C0013227 (UMLS CUI [4,2])
C0205314 (UMLS CUI [4,3])
Cardiac ejection fraction
Item
ef =< 40%
boolean
C0232174 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Condition Limiting Exercise | Congestive heart failure
Item
any condition (other than chf) that could limit exercise
boolean
C0348080 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0015259 (UMLS CUI [1,3])
C0018802 (UMLS CUI [2])
Comorbidity Probably Limiting Life Expectancy
Item
any concurrent disease likely to limit life expectancy.
boolean
C0009488 (UMLS CUI [1,1])
C0750492 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
C0023671 (UMLS CUI [1,4])
Study Subject Participation Status
Item
participation in another clinical trial
boolean
C2348568 (UMLS CUI [1])
primary valvular heart disease | Myocarditis | Hypertrophic Cardiomyopathy | Restrictive cardiomyopathy
Item
primary valvular disease, active myocarditis, or an obstructive or restrictive cardio-myopathy
boolean
C2064629 (UMLS CUI [1])
C0027059 (UMLS CUI [2])
C0007194 (UMLS CUI [3])
C0007196 (UMLS CUI [4])
Myocardial Infarction | Cerebrovascular accident | Angina, Unstable | Cardiac Surgery procedures
Item
heart attack, stroke, unstable angina or cardiac surgery within previous 3 months
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0018821 (UMLS CUI [4])
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