Engelsk

Eligibility Cardiovascular Disease Prevention NCT02239198

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
either taking no dietary supplements or willing to discontinue any dietary supplements for two weeks preceding the trial.
Beskrivning

Dietary Supplements Absent | Dietary Supplements Discontinue Willing

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0242295
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0242295
UMLS CUI [2,2]
C1444662
UMLS CUI [2,3]
C0600109
age >18 years
Beskrivning

Age

Datatyp

boolean

Alias
UMLS CUI [1]
C0001779
bmi <40
Beskrivning

Body mass index

Datatyp

boolean

Alias
UMLS CUI [1]
C1305855
blood pressure <140/90 mmhg, or stable blood pressure on medicines for past 3 months
Beskrivning

Blood pressure determination | Pharmaceutical Preparations Stable blood pressure

Datatyp

boolean

Alias
UMLS CUI [1]
C0005824
UMLS CUI [2,1]
C0013227
UMLS CUI [2,2]
C0428896
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
known diabetes mellitus according to the 2010 ada criteria, but pre-diabetic subjects with known impaired glucose tolerance (fasting glucose 101-125, and 2-hour post-prandial glucose level 141-200 mg/dl) can remain eligible.
Beskrivning

Diabetes Mellitus | Pre-diabetic Impaired glucose tolerance eligible | Glucose measurement, fasting | 2-hour postprandial blood glucose measurement

Datatyp

boolean

Alias
UMLS CUI [1]
C0011849
UMLS CUI [2,1]
C0362046
UMLS CUI [2,2]
C0271650
UMLS CUI [2,3]
C1548635
UMLS CUI [3]
C0202045
UMLS CUI [4]
C2238058
weight loss pharmacotherapy.
Beskrivning

Pharmacotherapy Weight loss

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0013216
UMLS CUI [1,2]
C1262477
lipid-lowering medication as this will alter the lipid profile being measured.
Beskrivning

Hypolipidemic Agents Affecting Lipid profile test

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0086440
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0850354
renal disease as this may affect blood pressure and dietary requirements.
Beskrivning

Kidney Disease Affecting Blood Pressure | Kidney Disease Affecting Dietary Requirements

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0022658
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0005823
UMLS CUI [2,1]
C0022658
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C1171332
smoking
Beskrivning

Tobacco use

Datatyp

boolean

Alias
UMLS CUI [1]
C0543414
pregnancy- a negative urine pregnancy test will be documented for any women participants of childbearing age prior to enrollment.
Beskrivning

Pregnancy | Childbearing Potential Urine pregnancy test negative

Datatyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2,1]
C3831118
UMLS CUI [2,2]
C0430057
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Similar models

Eligibility Cardiovascular Disease Prevention NCT02239198

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Dietary Supplements Absent | Dietary Supplements Discontinue Willing
Item
either taking no dietary supplements or willing to discontinue any dietary supplements for two weeks preceding the trial.
boolean
C0242295 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0242295 (UMLS CUI [2,1])
C1444662 (UMLS CUI [2,2])
C0600109 (UMLS CUI [2,3])
Age
Item
age >18 years
boolean
C0001779 (UMLS CUI [1])
Body mass index
Item
bmi <40
boolean
C1305855 (UMLS CUI [1])
Blood pressure determination | Pharmaceutical Preparations Stable blood pressure
Item
blood pressure <140/90 mmhg, or stable blood pressure on medicines for past 3 months
boolean
C0005824 (UMLS CUI [1])
C0013227 (UMLS CUI [2,1])
C0428896 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Diabetes Mellitus | Pre-diabetic Impaired glucose tolerance eligible | Glucose measurement, fasting | 2-hour postprandial blood glucose measurement
Item
known diabetes mellitus according to the 2010 ada criteria, but pre-diabetic subjects with known impaired glucose tolerance (fasting glucose 101-125, and 2-hour post-prandial glucose level 141-200 mg/dl) can remain eligible.
boolean
C0011849 (UMLS CUI [1])
C0362046 (UMLS CUI [2,1])
C0271650 (UMLS CUI [2,2])
C1548635 (UMLS CUI [2,3])
C0202045 (UMLS CUI [3])
C2238058 (UMLS CUI [4])
Pharmacotherapy Weight loss
Item
weight loss pharmacotherapy.
boolean
C0013216 (UMLS CUI [1,1])
C1262477 (UMLS CUI [1,2])
Hypolipidemic Agents Affecting Lipid profile test
Item
lipid-lowering medication as this will alter the lipid profile being measured.
boolean
C0086440 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0850354 (UMLS CUI [1,3])
Kidney Disease Affecting Blood Pressure | Kidney Disease Affecting Dietary Requirements
Item
renal disease as this may affect blood pressure and dietary requirements.
boolean
C0022658 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0005823 (UMLS CUI [1,3])
C0022658 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C1171332 (UMLS CUI [2,3])
Tobacco use
Item
smoking
boolean
C0543414 (UMLS CUI [1])
Pregnancy | Childbearing Potential Urine pregnancy test negative
Item
pregnancy- a negative urine pregnancy test will be documented for any women participants of childbearing age prior to enrollment.
boolean
C0032961 (UMLS CUI [1])
C3831118 (UMLS CUI [2,1])
C0430057 (UMLS CUI [2,2])
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