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)
  1. 6/6/17 6/6/17 -
  2. 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

English

Eligibility Primary Arterial Hypertension NCT00942487

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
aged 18 years or older, men and women, hospitalized and outpatients
Description

Age | Hospitalization | Outpatients

Data type

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2]
C0019993
UMLS CUI [3]
C0029921
with a history of primary arterial hypertension
Description

Essential Hypertension

Data type

boolean

Alias
UMLS CUI [1]
C0085580
with a daytime ambulatory blood pressure >140 and/or >90 mm hg
Description

Blood pressure ambulatory Daytime

Data type

boolean

Alias
UMLS CUI [1,1]
C0855316
UMLS CUI [1,2]
C0332169
with left ventricular hypertrophy: lvmi > 125 g/m2 for men, and > 110 g/m2 for women, by devereux formula, as recommended by the esh-esc guidelines (14)
Description

Left Ventricular Hypertrophy | Left ventricular mass Index | Gender

Data type

boolean

Alias
UMLS CUI [1]
C0149721
UMLS CUI [2,1]
C0455825
UMLS CUI [2,2]
C0918012
UMLS CUI [3]
C0079399
in sinus rhythm
Description

Sinus rhythm

Data type

boolean

Alias
UMLS CUI [1]
C0232201
consented, by signing the informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe arterial hypertension (systolic blood pressure > 180 mm hg and/or diastolic blood pressure > 110 mm hg)
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
any history of coronary heart disease (stable angina, acute coronary syndromes, myocardial infarction)
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
any history of cerebrovascular disease
Description

Cerebrovascular Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0007820
renal impairment (creatinine > 1.5 mg% for men, > 1.4 mg% for women)
Description

Renal Insufficiency | Creatinine measurement, serum | Gender

Data type

boolean

Alias
UMLS CUI [1]
C0201976
UMLS CUI [2]
C0079399
left ventricular global systolic dysfunction (ef < 45%)
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
more than mild valvar (mitral or aortic) regurgitation
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
hypertrophic cardiomyopathy
Description

Hypertrophic Cardiomyopathy

Data type

boolean

Alias
UMLS CUI [1]
C0007194
pericarditis
Description

Pericarditis

Data type

boolean

Alias
UMLS CUI [1]
C0031046
cor pulmonale
Description

Cor pulmonale

Data type

boolean

Alias
UMLS CUI [1]
C0034072
pregnancy or lactating women
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
any significant co-morbidities
Description

Comorbidity

Data type

boolean

Alias
UMLS CUI [1]
C0009488
contraindication to beta-blocker therapy
Description

Medical contraindication Adrenergic beta-1 Receptor Antagonists

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0304516
concomitant treatment with other beta-blockers
Description

Adrenergic beta-1 Receptor Antagonists

Data type

boolean

Alias
UMLS CUI [1]
C0304516
participation to another investigational study in the last 3 months
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Primary Arterial Hypertension NCT00942487

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age | Hospitalization | Outpatients
Item
aged 18 years or older, men and women, hospitalized and outpatients
boolean
C0001779 (UMLS CUI [1])
C0019993 (UMLS CUI [2])
C0029921 (UMLS CUI [3])
Essential Hypertension
Item
with a history of primary arterial hypertension
boolean
C0085580 (UMLS CUI [1])
Blood pressure ambulatory Daytime
Item
with a daytime ambulatory blood pressure >140 and/or >90 mm hg
boolean
C0855316 (UMLS CUI [1,1])
C0332169 (UMLS CUI [1,2])
Left Ventricular Hypertrophy | Left ventricular mass Index | Gender
Item
with left ventricular hypertrophy: lvmi > 125 g/m2 for men, and > 110 g/m2 for women, by devereux formula, as recommended by the esh-esc guidelines (14)
boolean
C0149721 (UMLS CUI [1])
C0455825 (UMLS CUI [2,1])
C0918012 (UMLS CUI [2,2])
C0079399 (UMLS CUI [3])
Sinus rhythm
Item
in sinus rhythm
boolean
C0232201 (UMLS CUI [1])
Informed Consent
Item
consented, by signing the informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Hypertensive disease Severe | Systolic Pressure | Diastolic blood pressure
Item
severe arterial hypertension (systolic blood pressure > 180 mm hg and/or diastolic blood pressure > 110 mm hg)
boolean
C0020538 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Coronary heart disease | Stable angina | Acute Coronary Syndrome | Myocardial Infarction
Item
any history of coronary heart disease (stable angina, acute coronary syndromes, myocardial infarction)
boolean
C0010068 (UMLS CUI [1])
C0340288 (UMLS CUI [2])
C0948089 (UMLS CUI [3])
C0027051 (UMLS CUI [4])
Cerebrovascular Disorders
Item
any history of cerebrovascular disease
boolean
C0007820 (UMLS CUI [1])
Renal Insufficiency | Creatinine measurement, serum | Gender
Item
renal impairment (creatinine > 1.5 mg% for men, > 1.4 mg% for women)
boolean
C0201976 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
Left ventricular systolic dysfunction Global | Cardiac ejection fraction
Item
left ventricular global systolic dysfunction (ef < 45%)
boolean
C1277187 (UMLS CUI [1,1])
C2348867 (UMLS CUI [1,2])
C0232174 (UMLS CUI [2])
Mitral Valve Insufficiency Moderate | Aortic Valve Insufficiency Moderate | Mitral Valve Insufficiency Severe | Aortic Valve Insufficiency Severe
Item
more than mild valvar (mitral or aortic) regurgitation
boolean
C0026266 (UMLS CUI [1,1])
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])
Hypertrophic Cardiomyopathy
Item
hypertrophic cardiomyopathy
boolean
C0007194 (UMLS CUI [1])
Pericarditis
Item
pericarditis
boolean
C0031046 (UMLS CUI [1])
Cor pulmonale
Item
cor pulmonale
boolean
C0034072 (UMLS CUI [1])
Pregnancy | Breast Feeding
Item
pregnancy or lactating women
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Comorbidity
Item
any significant co-morbidities
boolean
C0009488 (UMLS CUI [1])
Medical contraindication Adrenergic beta-1 Receptor Antagonists
Item
contraindication to beta-blocker therapy
boolean
C1301624 (UMLS CUI [1,1])
C0304516 (UMLS CUI [1,2])
Adrenergic beta-1 Receptor Antagonists
Item
concomitant treatment with other beta-blockers
boolean
C0304516 (UMLS CUI [1])
Study Subject Participation Status
Item
participation to another investigational study in the last 3 months
boolean
C2348568 (UMLS CUI [1])
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