Eligibility Hypertension NCT00781365

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age 21 years or more
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
linked using emr data to a healthpartners medical group primary care clinic
Description

Use of Electronic Health Records | Clinic / Center - Primary Care

Data type

boolean

Alias
UMLS CUI [1,1]
C1524063
UMLS CUI [1,2]
C2362543
UMLS CUI [2]
C1552443
within the 12-month period of time prior to screening have had at least 2 primary care outpatient encounters, in the two most recent of which the blood pressure was above joint national committee 7 (jnc7) goal (<140/90 mmhg or <130/80 for patients with diabetes or kidney disease).
Description

Primary Care Outpatient Encounter Quantity | Blood pressure determination | Diabetes Mellitus | Kidney Disease

Data type

boolean

Alias
UMLS CUI [1,1]
C0033137
UMLS CUI [1,2]
C0029921
UMLS CUI [1,3]
C1947978
UMLS CUI [1,4]
C1265611
UMLS CUI [2]
C0005824
UMLS CUI [3]
C0011849
UMLS CUI [4]
C0022658
have a measured blood pressure at a research clinic screening visit above the jnc7 goal
Description

Increase in blood pressure

Data type

boolean

Alias
UMLS CUI [1]
C0497247
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
acute coronary syndrome or stroke within the past 3 months
Description

Acute Coronary Syndrome | Cerebrovascular accident

Data type

boolean

Alias
UMLS CUI [1]
C0948089
UMLS CUI [2]
C0038454
class iii (marked limitation of physical activity) or iv (symptoms at rest) new york heart association heart failure, or known left ventricular ejection fraction (<30%)
Description

Heart failure New York Heart Association Classification | Left ventricular ejection fraction

Data type

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
UMLS CUI [2]
C0428772
severe renal dysfunction, with epidermal growth factor receptor (egfr) ,30 ml/min/1.73 m2 using the abbreviated modification of diet in renal disease study (mdrd) equation
Description

Renal dysfunction Severe | GFR estimation by MDRD

Data type

boolean

Alias
UMLS CUI [1,1]
C3279454
UMLS CUI [1,2]
C0205082
UMLS CUI [2]
C2170215
known secondary causes of hypertension such as coarctation of the aorta, pheochromocytoma, adrenal cortical hypertension or renal vascular hypertension
Description

Secondary hypertension | Aortic coarctation | Pheochromocytoma | Adrenal Cortex Hypertension | Hypertension, Renovascular

Data type

boolean

Alias
UMLS CUI [1]
C0155616
UMLS CUI [2]
C0003492
UMLS CUI [3]
C0031511
UMLS CUI [4,1]
C0001613
UMLS CUI [4,2]
C0020538
UMLS CUI [5]
C0020545
unwillingness to be followed for a period of 18 months
Description

Follow-up Unwilling

Data type

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C0558080
pregnancy or unwillingness to use reliable bith control for females of child-bearing age
Description

Pregnancy | Childbearing Potential Contraceptive methods Unwilling

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2,1]
C3831118
UMLS CUI [2,2]
C0700589
UMLS CUI [2,3]
C0558080
participation in another clinical trial
Description

Study Subject Participation Status | Clinical Trial

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0008976
requires an interpreter to communicate with health care providers
Description

Communication Health Personnel | Need for interpreter

Data type

boolean

Alias
UMLS CUI [1,1]
C0009452
UMLS CUI [1,2]
C0018724
UMLS CUI [2]
C1278519
dementia, mental illness or any condition that would limit ability to give informed consent
Description

Dementia | Mental disorders | Condition Limiting Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0497327
UMLS CUI [2]
C0004936
UMLS CUI [3,1]
C0348080
UMLS CUI [3,2]
C0439801
UMLS CUI [3,3]
C0021430

Similar models

Eligibility Hypertension NCT00781365

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age 21 years or more
boolean
C0001779 (UMLS CUI [1])
Use of Electronic Health Records | Clinic / Center - Primary Care
Item
linked using emr data to a healthpartners medical group primary care clinic
boolean
C1524063 (UMLS CUI [1,1])
C2362543 (UMLS CUI [1,2])
C1552443 (UMLS CUI [2])
Primary Care Outpatient Encounter Quantity | Blood pressure determination | Diabetes Mellitus | Kidney Disease
Item
within the 12-month period of time prior to screening have had at least 2 primary care outpatient encounters, in the two most recent of which the blood pressure was above joint national committee 7 (jnc7) goal (<140/90 mmhg or <130/80 for patients with diabetes or kidney disease).
boolean
C0033137 (UMLS CUI [1,1])
C0029921 (UMLS CUI [1,2])
C1947978 (UMLS CUI [1,3])
C1265611 (UMLS CUI [1,4])
C0005824 (UMLS CUI [2])
C0011849 (UMLS CUI [3])
C0022658 (UMLS CUI [4])
Increase in blood pressure
Item
have a measured blood pressure at a research clinic screening visit above the jnc7 goal
boolean
C0497247 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Acute Coronary Syndrome | Cerebrovascular accident
Item
acute coronary syndrome or stroke within the past 3 months
boolean
C0948089 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
Heart failure New York Heart Association Classification | Left ventricular ejection fraction
Item
class iii (marked limitation of physical activity) or iv (symptoms at rest) new york heart association heart failure, or known left ventricular ejection fraction (<30%)
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C0428772 (UMLS CUI [2])
Renal dysfunction Severe | GFR estimation by MDRD
Item
severe renal dysfunction, with epidermal growth factor receptor (egfr) ,30 ml/min/1.73 m2 using the abbreviated modification of diet in renal disease study (mdrd) equation
boolean
C3279454 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C2170215 (UMLS CUI [2])
Secondary hypertension | Aortic coarctation | Pheochromocytoma | Adrenal Cortex Hypertension | Hypertension, Renovascular
Item
known secondary causes of hypertension such as coarctation of the aorta, pheochromocytoma, adrenal cortical hypertension or renal vascular hypertension
boolean
C0155616 (UMLS CUI [1])
C0003492 (UMLS CUI [2])
C0031511 (UMLS CUI [3])
C0001613 (UMLS CUI [4,1])
C0020538 (UMLS CUI [4,2])
C0020545 (UMLS CUI [5])
Follow-up Unwilling
Item
unwillingness to be followed for a period of 18 months
boolean
C3274571 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])
Pregnancy | Childbearing Potential Contraceptive methods Unwilling
Item
pregnancy or unwillingness to use reliable bith control for females of child-bearing age
boolean
C0032961 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
Study Subject Participation Status | Clinical Trial
Item
participation in another clinical trial
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2])
Communication Health Personnel | Need for interpreter
Item
requires an interpreter to communicate with health care providers
boolean
C0009452 (UMLS CUI [1,1])
C0018724 (UMLS CUI [1,2])
C1278519 (UMLS CUI [2])
Dementia | Mental disorders | Condition Limiting Informed Consent
Item
dementia, mental illness or any condition that would limit ability to give informed consent
boolean
C0497327 (UMLS CUI [1])
C0004936 (UMLS CUI [2])
C0348080 (UMLS CUI [3,1])
C0439801 (UMLS CUI [3,2])
C0021430 (UMLS CUI [3,3])