Eligibility Hypertension NCT02362893

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
18 years and above
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
residing in oslo/akershus
Description

Resident Norway

Type de données

boolean

Alias
UMLS CUI [1,1]
C2347958
UMLS CUI [1,2]
C0028423
ambulatory systolic daytime blood pressure ≥ 135 mmhg
Description

Systolic Pressure Ambulatory Daytime

Type de données

boolean

Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0439841
UMLS CUI [1,3]
C0332169
≥ 2 antihypertensive medications
Description

Antihypertensive Agents

Type de données

boolean

Alias
UMLS CUI [1]
C0003364
be able to read and write norwegian
Description

Able to read Norwegian language | Able to write Norwegian language

Type de données

boolean

Alias
UMLS CUI [1,1]
C0586740
UMLS CUI [1,2]
C0028424
UMLS CUI [2,1]
C0584993
UMLS CUI [2,2]
C0028424
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
critical illness, ongoing treatment
Description

Critical Illness | Therapeutic procedure Continuous

Type de données

boolean

Alias
UMLS CUI [1]
C0010340
UMLS CUI [2,1]
C0087111
UMLS CUI [2,2]
C0549178
known atrial fibrillation
Description

Atrial Fibrillation

Type de données

boolean

Alias
UMLS CUI [1]
C0004238
known heart valve stenosis
Description

Heart valve stenosis

Type de données

boolean

Alias
UMLS CUI [1]
C0264878
myocardial infarction, angina pectoris or stroke the past 6 months
Description

Myocardial Infarction | Angina Pectoris | Cerebrovascular accident

Type de données

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0002962
UMLS CUI [3]
C0038454
known severe renal impairment (egfr < 30 ml/min/1.73 m2)
Description

Renal Insufficiency Severe | Estimated Glomerular Filtration Rate

Type de données

boolean

Alias
UMLS CUI [1,1]
C1565489
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C3811844
history of dot prior to abpm
Description

Directly Observed Therapy prior to Blood Pressure Monitoring, Ambulatory

Type de données

boolean

Alias
UMLS CUI [1,1]
C0872145
UMLS CUI [1,2]
C0332152
UMLS CUI [1,3]
C0242876
participation in other interventional study
Description

Study Subject Participation Status

Type de données

boolean

Alias
UMLS CUI [1]
C2348568

Similar models

Eligibility Hypertension NCT02362893

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
18 years and above
boolean
C0001779 (UMLS CUI [1])
Resident Norway
Item
residing in oslo/akershus
boolean
C2347958 (UMLS CUI [1,1])
C0028423 (UMLS CUI [1,2])
Systolic Pressure Ambulatory Daytime
Item
ambulatory systolic daytime blood pressure ≥ 135 mmhg
boolean
C0871470 (UMLS CUI [1,1])
C0439841 (UMLS CUI [1,2])
C0332169 (UMLS CUI [1,3])
Antihypertensive Agents
Item
≥ 2 antihypertensive medications
boolean
C0003364 (UMLS CUI [1])
Able to read Norwegian language | Able to write Norwegian language
Item
be able to read and write norwegian
boolean
C0586740 (UMLS CUI [1,1])
C0028424 (UMLS CUI [1,2])
C0584993 (UMLS CUI [2,1])
C0028424 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Critical Illness | Therapeutic procedure Continuous
Item
critical illness, ongoing treatment
boolean
C0010340 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C0549178 (UMLS CUI [2,2])
Atrial Fibrillation
Item
known atrial fibrillation
boolean
C0004238 (UMLS CUI [1])
Heart valve stenosis
Item
known heart valve stenosis
boolean
C0264878 (UMLS CUI [1])
Myocardial Infarction | Angina Pectoris | Cerebrovascular accident
Item
myocardial infarction, angina pectoris or stroke the past 6 months
boolean
C0027051 (UMLS CUI [1])
C0002962 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
Renal Insufficiency Severe | Estimated Glomerular Filtration Rate
Item
known severe renal impairment (egfr < 30 ml/min/1.73 m2)
boolean
C1565489 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C3811844 (UMLS CUI [2])
Directly Observed Therapy prior to Blood Pressure Monitoring, Ambulatory
Item
history of dot prior to abpm
boolean
C0872145 (UMLS CUI [1,1])
C0332152 (UMLS CUI [1,2])
C0242876 (UMLS CUI [1,3])
Study Subject Participation Status
Item
participation in other interventional study
boolean
C2348568 (UMLS CUI [1])