Engelsk

Eligibility Cardiovascular Disease NCT00685581

1 Formulär  
Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
hdl cholesterol, g/l > 0.4
Beskrivning

Serum HDL cholesterol measurement

Datatyp

boolean

Alias
UMLS CUI [1]
C0428472
triacylglycerol g/l <1.50
Beskrivning

Triglycerides

Datatyp

boolean

Alias
UMLS CUI [1]
C0041004
ldl cholesterol g/l <1.60
Beskrivning

Serum LDL cholesterol measurement

Datatyp

boolean

Alias
UMLS CUI [1]
C0428474
waist size < 94 cm (men) or 80 cm (women)
Beskrivning

Waist Circumference | Gender

Datatyp

boolean

Alias
UMLS CUI [1]
C0455829
UMLS CUI [2]
C0079399
affiliated to national health insurance
Beskrivning

National Health Insurance Affiliated

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0027452
UMLS CUI [1,2]
C1510826
normal blood pressure (diastolic <90 mm hg, systolic <140 mm hg)
Beskrivning

Normal blood pressure | Diastolic blood pressure | Systolic Pressure

Datatyp

boolean

Alias
UMLS CUI [1]
C2712122
UMLS CUI [2]
C0428883
UMLS CUI [3]
C0871470
for women: effective contraception
Beskrivning

Gender Contraceptive methods

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0079399
UMLS CUI [1,2]
C0700589
subject giving his/her written informed consent
Beskrivning

Informed Consent

Datatyp

boolean

Alias
UMLS CUI [1]
C0021430
subject willing to comply with the study procedures
Beskrivning

Protocol Compliance

Datatyp

boolean

Alias
UMLS CUI [1]
C0525058
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
reported food allergies
Beskrivning

Food Allergy

Datatyp

boolean

Alias
UMLS CUI [1]
C0016470
currently participating or having participated in another clinical trial during the last 4 weeks prior to the beginning of this study
Beskrivning

Study Subject Participation Status

Datatyp

boolean

Alias
UMLS CUI [1]
C2348568
hepatic or renal impairments
Beskrivning

Hepatic impairment | Renal Insufficiency

Datatyp

boolean

Alias
UMLS CUI [1]
C0948807
UMLS CUI [2]
C1565489
positive serologies to hiv or hcv,
Beskrivning

HIV Seropositivity | Hepatitis C virus Serology positive

Datatyp

boolean

Alias
UMLS CUI [1]
C0019699
UMLS CUI [2,1]
C0220847
UMLS CUI [2,2]
C0242089
blood donation done less than 2 months before the start of the study
Beskrivning

Blood Donation

Datatyp

boolean

Alias
UMLS CUI [1]
C0005794
chronic pathologies
Beskrivning

Chronic disease

Datatyp

boolean

Alias
UMLS CUI [1]
C0008679
refusal to be registered on the national volunteers data file
Beskrivning

Volunteers National Data File | Enrollment Refused

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1708335
UMLS CUI [1,2]
C0015737
UMLS CUI [1,3]
C0242193
UMLS CUI [2,1]
C1516879
UMLS CUI [2,2]
C1705116
being in exclusion on the national volunteers data file
Beskrivning

Volunteers National Data File | Patient Excluded

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1708335
UMLS CUI [1,2]
C0015737
UMLS CUI [1,3]
C0242193
UMLS CUI [2,1]
C0030705
UMLS CUI [2,2]
C2828389
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Similar models

Eligibility Cardiovascular Disease NCT00685581

1 Formulär
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Serum HDL cholesterol measurement
Item
hdl cholesterol, g/l > 0.4
boolean
C0428472 (UMLS CUI [1])
Triglycerides
Item
triacylglycerol g/l <1.50
boolean
C0041004 (UMLS CUI [1])
Serum LDL cholesterol measurement
Item
ldl cholesterol g/l <1.60
boolean
C0428474 (UMLS CUI [1])
Waist Circumference | Gender
Item
waist size < 94 cm (men) or 80 cm (women)
boolean
C0455829 (UMLS CUI [1])
C0079399 (UMLS CUI [2])
National Health Insurance Affiliated
Item
affiliated to national health insurance
boolean
C0027452 (UMLS CUI [1,1])
C1510826 (UMLS CUI [1,2])
Normal blood pressure | Diastolic blood pressure | Systolic Pressure
Item
normal blood pressure (diastolic <90 mm hg, systolic <140 mm hg)
boolean
C2712122 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
C0871470 (UMLS CUI [3])
Gender Contraceptive methods
Item
for women: effective contraception
boolean
C0079399 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
Informed Consent
Item
subject giving his/her written informed consent
boolean
C0021430 (UMLS CUI [1])
Protocol Compliance
Item
subject willing to comply with the study procedures
boolean
C0525058 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Food Allergy
Item
reported food allergies
boolean
C0016470 (UMLS CUI [1])
Study Subject Participation Status
Item
currently participating or having participated in another clinical trial during the last 4 weeks prior to the beginning of this study
boolean
C2348568 (UMLS CUI [1])
Hepatic impairment | Renal Insufficiency
Item
hepatic or renal impairments
boolean
C0948807 (UMLS CUI [1])
C1565489 (UMLS CUI [2])
HIV Seropositivity | Hepatitis C virus Serology positive
Item
positive serologies to hiv or hcv,
boolean
C0019699 (UMLS CUI [1])
C0220847 (UMLS CUI [2,1])
C0242089 (UMLS CUI [2,2])
Blood Donation
Item
blood donation done less than 2 months before the start of the study
boolean
C0005794 (UMLS CUI [1])
Chronic disease
Item
chronic pathologies
boolean
C0008679 (UMLS CUI [1])
Volunteers National Data File | Enrollment Refused
Item
refusal to be registered on the national volunteers data file
boolean
C1708335 (UMLS CUI [1,1])
C0015737 (UMLS CUI [1,2])
C0242193 (UMLS CUI [1,3])
C1516879 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Volunteers National Data File | Patient Excluded
Item
being in exclusion on the national volunteers data file
boolean
C1708335 (UMLS CUI [1,1])
C0015737 (UMLS CUI [1,2])
C0242193 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
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