ID

19773

Description

Home Blood Pressure-guided Antihypertensive Intervention for Elderly (HBP-GUIDE) Study; ODM derived from: https://clinicaltrials.gov/show/NCT00334724

Link

https://clinicaltrials.gov/show/NCT00334724

Keywords

Versions (1)
  1. 1/27/17 1/27/17 -
Uploaded on

January 27, 2017

DOI

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License

Creative Commons BY 4.0
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Eligibility Cardiovascular Disease NCT00334724

English

Eligibility Cardiovascular Disease NCT00334724

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
outpatients aged over 65 years and less than 80 years
Description

Outpatients | Age

Data type

boolean

Alias
UMLS CUI [1]
C0029921
UMLS CUI [2]
C0001779
patients with a stable seated systolic blood pressure of ≥ 140 mmhg or diastolic blood pressure of ≥ 90 mmhg at two visits within 8 weeks
Description

Systolic Pressure Stable | Diastolic blood pressure Stable

Data type

boolean

Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0205360
UMLS CUI [2,1]
C0428883
UMLS CUI [2,2]
C0205360
patients with a stable seated systolic blood pressure of ≥ 135 mmhg or diastolic blood pressure of ≥ 85 mmhg at home (home blood pressure is measured every morning within 1 h of waking, and defined as the mean of 3 days measurement within 8 weeks)
Description

Average home systolic blood pressure | Average home diastolic blood pressure

Data type

boolean

Alias
UMLS CUI [1]
C1531726
UMLS CUI [2]
C1531725
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with secondary hypertension or malignant hypertension
Description

Secondary hypertension | Malignant Hypertension

Data type

boolean

Alias
UMLS CUI [1]
C0155616
UMLS CUI [2]
C0020540
patients with a stable seated systolic pressure of ≥ 180 mmhg or diastolic pressure of ≥ 110 mmhg
Description

Systolic Pressure Stable | Diastolic blood pressure Stable

Data type

boolean

Alias
UMLS CUI [1,1]
C0871470
UMLS CUI [1,2]
C0205360
UMLS CUI [2,1]
C0428883
UMLS CUI [2,2]
C0205360
patients with renal dysfunction with a serum creatinine level of ≥ 2 mg/dl
Description

Renal dysfunction | Creatinine measurement, serum

Data type

boolean

Alias
UMLS CUI [1]
C3279454
UMLS CUI [2]
C0201976
patients with liver dysfunction
Description

Liver Dysfunction

Data type

boolean

Alias
UMLS CUI [1]
C0086565
patients with a history of hypersensitivity to angiotensin ii receptor blockade
Description

Hypersensitivity Angiotensin II receptor antagonist

Data type

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0521942
patients with a history of myocardial infarction within 6 months prior to enrolment in the study
Description

Myocardial Infarction

Data type

boolean

Alias
UMLS CUI [1]
C0027051
patients who underwent coronary arterioplasty within 6 months prior to enrolment in the study or patients who will undergo coronary arterioplasty within 6 months after entry
Description

Coronary angioplasty

Data type

boolean

Alias
UMLS CUI [1]
C0190211
patients with heart failure
Description

Heart failure

Data type

boolean

Alias
UMLS CUI [1]
C0018801
patients with a history of cerebrovascular disorder
Description

Cerebrovascular Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0007820
other patients who are judged to be inappropriate for the study by the investigator
Description

Patients Inappropriate Clinical Trial

Data type

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1548788
UMLS CUI [1,3]
C0008976
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Similar models

Eligibility Cardiovascular Disease NCT00334724

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Outpatients | Age
Item
outpatients aged over 65 years and less than 80 years
boolean
C0029921 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Systolic Pressure Stable | Diastolic blood pressure Stable
Item
patients with a stable seated systolic blood pressure of ≥ 140 mmhg or diastolic blood pressure of ≥ 90 mmhg at two visits within 8 weeks
boolean
C0871470 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0428883 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
Average home systolic blood pressure | Average home diastolic blood pressure
Item
patients with a stable seated systolic blood pressure of ≥ 135 mmhg or diastolic blood pressure of ≥ 85 mmhg at home (home blood pressure is measured every morning within 1 h of waking, and defined as the mean of 3 days measurement within 8 weeks)
boolean
C1531726 (UMLS CUI [1])
C1531725 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Secondary hypertension | Malignant Hypertension
Item
patients with secondary hypertension or malignant hypertension
boolean
C0155616 (UMLS CUI [1])
C0020540 (UMLS CUI [2])
Systolic Pressure Stable | Diastolic blood pressure Stable
Item
patients with a stable seated systolic pressure of ≥ 180 mmhg or diastolic pressure of ≥ 110 mmhg
boolean
C0871470 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0428883 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
Renal dysfunction | Creatinine measurement, serum
Item
patients with renal dysfunction with a serum creatinine level of ≥ 2 mg/dl
boolean
C3279454 (UMLS CUI [1])
C0201976 (UMLS CUI [2])
Liver Dysfunction
Item
patients with liver dysfunction
boolean
C0086565 (UMLS CUI [1])
Hypersensitivity Angiotensin II receptor antagonist
Item
patients with a history of hypersensitivity to angiotensin ii receptor blockade
boolean
C0020517 (UMLS CUI [1,1])
C0521942 (UMLS CUI [1,2])
Myocardial Infarction
Item
patients with a history of myocardial infarction within 6 months prior to enrolment in the study
boolean
C0027051 (UMLS CUI [1])
Coronary angioplasty
Item
patients who underwent coronary arterioplasty within 6 months prior to enrolment in the study or patients who will undergo coronary arterioplasty within 6 months after entry
boolean
C0190211 (UMLS CUI [1])
Heart failure
Item
patients with heart failure
boolean
C0018801 (UMLS CUI [1])
Cerebrovascular Disorders
Item
patients with a history of cerebrovascular disorder
boolean
C0007820 (UMLS CUI [1])
Patients Inappropriate Clinical Trial
Item
other patients who are judged to be inappropriate for the study by the investigator
boolean
C0030705 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
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