Information:
Fel:
ID
39538
Beskrivning
Prednisone for Heart Failure Patients With Hyperuricemia; ODM derived from: https://clinicaltrials.gov/show/NCT02129764
Länk
https://clinicaltrials.gov/show/NCT02129764
Nyckelord
Versioner (1)
- 2020-01-25 2020-01-25 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
25 januari 2020
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Heart Failure, Hyperuricemia NCT02129764
Eligibility Heart Failure, Hyperuricemia NCT02129764
- StudyEvent: Eligibility
Similar models
Eligibility Heart Failure, Hyperuricemia NCT02129764
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Chronic congestive heart failure
Item
chronic congestive heart failure
boolean
C0264722 (UMLS CUI [1])
Age
Item
18-80 years old
boolean
C0001779 (UMLS CUI [1])
New York Heart Association Classification
Item
nyha class ii-iv
boolean
C1275491 (UMLS CUI [1])
Serum uric acid measurement
Item
serum uric acid > 7mg/dl
boolean
C0455272 (UMLS CUI [1])
Left ventricular ejection fraction
Item
left ventricular ejection fraction ≤ 45%
boolean
C0428772 (UMLS CUI [1])
Arthritis, Gouty
Item
acute gouty arthritis;
boolean
C0003868 (UMLS CUI [1])
Condition Limiting Prednisone | Condition Limiting Xanthine Oxidase Inhibitors
Item
any condition (other than heart failure) that could limit the use of prednisone or xanthine oxidase inhibitors;
boolean
C0348080 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0032952 (UMLS CUI [1,3])
C0348080 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0302609 (UMLS CUI [2,3])
C0439801 (UMLS CUI [1,2])
C0032952 (UMLS CUI [1,3])
C0348080 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0302609 (UMLS CUI [2,3])
Decompensated cardiac failure
Item
acute decompensated heart failure;
boolean
C0581377 (UMLS CUI [1])
Comorbidity Limiting Life Expectancy
Item
any concurrent disease that likely limits life expectancy;
boolean
C0009488 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0023671 (UMLS CUI [1,3])
C0439801 (UMLS CUI [1,2])
C0023671 (UMLS CUI [1,3])
Myocarditis | Hypertrophic Cardiomyopathy | Restrictive cardiomyopathy
Item
active myocarditis, or an hypertrophic obstructive or restrictive cardiomyopathy;
boolean
C0027059 (UMLS CUI [1])
C0007194 (UMLS CUI [2])
C0007196 (UMLS CUI [3])
C0007194 (UMLS CUI [2])
C0007196 (UMLS CUI [3])
Myocardial Infarction | Cerebrovascular accident | Angina, Unstable | Cardiac Surgery
Item
myocardial infarction, stroke, unstable angina, or cardiac surgery within the previous 3 months;
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0018821 (UMLS CUI [4])
C0038454 (UMLS CUI [2])
C0002965 (UMLS CUI [3])
C0018821 (UMLS CUI [4])
Indication Hemodialysis
Item
indication for hemodialysis
boolean
C3146298 (UMLS CUI [1,1])
C0019004 (UMLS CUI [1,2])
C0019004 (UMLS CUI [1,2])
Creatinine measurement, serum
Item
creatinine> 3.0 mg per deciliter at admission to the hospital
boolean
C0201976 (UMLS CUI [1])
Systolic Pressure Uncontrolled
Item
uncontrolled systolic blood pressure > 160 mmhg
boolean
C0871470 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0205318 (UMLS CUI [1,2])
Bilateral renal artery stenosis
Item
known bilateral renal artery stenosis
boolean
C0856760 (UMLS CUI [1])
Complex congenital heart disease
Item
complex congenital heart disease
boolean
C0744669 (UMLS CUI [1])
Signs Communicable Diseases
Item
any signs of infections
boolean
C0311392 (UMLS CUI [1,1])
C0009450 (UMLS CUI [1,2])
C0009450 (UMLS CUI [1,2])
Study Subject Participation Status | Clinical Trial Involving Intervention
Item
enrollment in another clinical trial involving medical or device-based interventions
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2,1])
C1314939 (UMLS CUI [2,2])
C0184661 (UMLS CUI [2,3])
C0008976 (UMLS CUI [2,1])
C1314939 (UMLS CUI [2,2])
C0184661 (UMLS CUI [2,3])