ID
22673
Description
Effects of Nebivolol on Subclinical Left Ventricular dySfunction: A Comparative Study Against Metoprolol; ODM derived from: https://clinicaltrials.gov/show/NCT00942487
Link
https://clinicaltrials.gov/show/NCT00942487
Keywords
Versions (2)
- 6/6/17 6/6/17 -
- 6/9/17 6/9/17 - Julian Varghese
Uploaded on
June 9, 2017
DOI
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License
Creative Commons BY 4.0
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Eligibility Primary Arterial Hypertension NCT00942487
Eligibility Primary Arterial Hypertension NCT00942487
- StudyEvent: Eligibility
Description
Exclusion Criteria
Alias
- UMLS CUI
- C0680251
Description
Hypertensive disease Severe | Systolic Pressure | Diastolic blood pressure
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0020538
- UMLS CUI [1,2]
- C0205082
- UMLS CUI [2]
- C0871470
- UMLS CUI [3]
- C0428883
Description
Coronary heart disease | Stable angina | Acute Coronary Syndrome | Myocardial Infarction
Data type
boolean
Alias
- UMLS CUI [1]
- C0010068
- UMLS CUI [2]
- C0340288
- UMLS CUI [3]
- C0948089
- UMLS CUI [4]
- C0027051
Description
Cerebrovascular Disorders
Data type
boolean
Alias
- UMLS CUI [1]
- C0007820
Description
Renal Insufficiency | Creatinine measurement, serum | Gender
Data type
boolean
Alias
- UMLS CUI [1]
- C0201976
- UMLS CUI [2]
- C0079399
Description
Left ventricular systolic dysfunction Global | Cardiac ejection fraction
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1277187
- UMLS CUI [1,2]
- C2348867
- UMLS CUI [2]
- C0232174
Description
Mitral Valve Insufficiency Moderate | Aortic Valve Insufficiency Moderate | Mitral Valve Insufficiency Severe | Aortic Valve Insufficiency Severe
Data type
boolean
Alias
- UMLS CUI [1,1]
- C0026266
- UMLS CUI [1,2]
- C0205081
- UMLS CUI [2,1]
- C0003504
- UMLS CUI [2,2]
- C0205081
- UMLS CUI [3,1]
- C0026266
- UMLS CUI [3,2]
- C0205082
- UMLS CUI [4,1]
- C0003504
- UMLS CUI [4,2]
- C0205082
Description
Hypertrophic Cardiomyopathy
Data type
boolean
Alias
- UMLS CUI [1]
- C0007194
Description
Pericarditis
Data type
boolean
Alias
- UMLS CUI [1]
- C0031046
Description
Cor pulmonale
Data type
boolean
Alias
- UMLS CUI [1]
- C0034072
Description
Pregnancy | Breast Feeding
Data type
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
Description
Comorbidity
Data type
boolean
Alias
- UMLS CUI [1]
- C0009488
Description
Medical contraindication Adrenergic beta-1 Receptor Antagonists
Data type
boolean
Alias
- UMLS CUI [1,1]
- C1301624
- UMLS CUI [1,2]
- C0304516
Description
Adrenergic beta-1 Receptor Antagonists
Data type
boolean
Alias
- UMLS CUI [1]
- C0304516
Description
Study Subject Participation Status
Data type
boolean
Alias
- UMLS CUI [1]
- C2348568
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Eligibility Primary Arterial Hypertension NCT00942487
- StudyEvent: Eligibility
C0019993 (UMLS CUI [2])
C0029921 (UMLS CUI [3])
C0332169 (UMLS CUI [1,2])
C0455825 (UMLS CUI [2,1])
C0918012 (UMLS CUI [2,2])
C0079399 (UMLS CUI [3])
C0205082 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
C0340288 (UMLS CUI [2])
C0948089 (UMLS CUI [3])
C0027051 (UMLS CUI [4])
C0079399 (UMLS CUI [2])
C2348867 (UMLS CUI [1,2])
C0232174 (UMLS CUI [2])
C0205081 (UMLS CUI [1,2])
C0003504 (UMLS CUI [2,1])
C0205081 (UMLS CUI [2,2])
C0026266 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0003504 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0006147 (UMLS CUI [2])
C0304516 (UMLS CUI [1,2])