Eligibility Hypertension NCT00648895

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
male or female, ambulatory outpatients 18-79 years old at screening
Beschreibung

Outpatients Ambulatory | Age

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0029921
UMLS CUI [1,2]
C1561561
UMLS CUI [2]
C0001779
minimum 2-year history of stage i/ii hypertension
Beschreibung

Hypertensive disease Stage Disease length

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020538
UMLS CUI [1,2]
C1306673
UMLS CUI [1,3]
C0872146
qualifying blood pressure criteria for study entry and for randomization
Beschreibung

Blood pressure measurement

Datentyp

boolean

Alias
UMLS CUI [1]
C0005824
willing to adhere to the dietary compliance and undergo protocol procedures
Beschreibung

Compliance behavior Dietary | Protocol Compliance

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0012155
UMLS CUI [2]
C0525058
have a lifestyle that will permit him/her to attend all evaluations, including those conducted on consecutive days
Beschreibung

Life Style allowing Evaluation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0023676
UMLS CUI [1,2]
C0683607
UMLS CUI [1,3]
C1261322
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
have any form of secondary hypertension
Beschreibung

Secondary hypertension

Datentyp

boolean

Alias
UMLS CUI [1]
C0155616
have clinically significant respiratory or cardiovascular disease
Beschreibung

Respiration Disorders | Cardiovascular Diseases

Datentyp

boolean

Alias
UMLS CUI [1]
C0035204
UMLS CUI [2]
C0007222
presence/history of coronary artery disease or peripheral vascular disease
Beschreibung

Coronary Artery Disease | Peripheral Vascular Diseases

Datentyp

boolean

Alias
UMLS CUI [1]
C1956346
UMLS CUI [2]
C0085096
have diabetes mellitus, type i or ii
Beschreibung

Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent

Datentyp

boolean

Alias
UMLS CUI [1]
C0011854
UMLS CUI [2]
C0011860
have a history of hypersensitivity to nebivolol, metoprolol, or any beta-blocker
Beschreibung

Hypersensitivity nebivolol | Metoprolol allergy | BETA BLOCKER ALLERGY

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0068475
UMLS CUI [2]
C0570889
UMLS CUI [3]
C0741466

Ähnliche Modelle

Eligibility Hypertension NCT00648895

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Outpatients Ambulatory | Age
Item
male or female, ambulatory outpatients 18-79 years old at screening
boolean
C0029921 (UMLS CUI [1,1])
C1561561 (UMLS CUI [1,2])
C0001779 (UMLS CUI [2])
Hypertensive disease Stage Disease length
Item
minimum 2-year history of stage i/ii hypertension
boolean
C0020538 (UMLS CUI [1,1])
C1306673 (UMLS CUI [1,2])
C0872146 (UMLS CUI [1,3])
Blood pressure measurement
Item
qualifying blood pressure criteria for study entry and for randomization
boolean
C0005824 (UMLS CUI [1])
Compliance behavior Dietary | Protocol Compliance
Item
willing to adhere to the dietary compliance and undergo protocol procedures
boolean
C1321605 (UMLS CUI [1,1])
C0012155 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2])
Life Style allowing Evaluation
Item
have a lifestyle that will permit him/her to attend all evaluations, including those conducted on consecutive days
boolean
C0023676 (UMLS CUI [1,1])
C0683607 (UMLS CUI [1,2])
C1261322 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Secondary hypertension
Item
have any form of secondary hypertension
boolean
C0155616 (UMLS CUI [1])
Respiration Disorders | Cardiovascular Diseases
Item
have clinically significant respiratory or cardiovascular disease
boolean
C0035204 (UMLS CUI [1])
C0007222 (UMLS CUI [2])
Coronary Artery Disease | Peripheral Vascular Diseases
Item
presence/history of coronary artery disease or peripheral vascular disease
boolean
C1956346 (UMLS CUI [1])
C0085096 (UMLS CUI [2])
Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent
Item
have diabetes mellitus, type i or ii
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
Hypersensitivity nebivolol | Metoprolol allergy | BETA BLOCKER ALLERGY
Item
have a history of hypersensitivity to nebivolol, metoprolol, or any beta-blocker
boolean
C0020517 (UMLS CUI [1,1])
C0068475 (UMLS CUI [1,2])
C0570889 (UMLS CUI [2])
C0741466 (UMLS CUI [3])