Informações:
Falhas:
ID
23723
Descrição
Impact of Vaccenic Acid Consumption on the Metabolism of Saturated Fatty Acids: Relationship With Cardiovascular Risk Factors; ODM derived from: https://clinicaltrials.gov/show/NCT00685581
Link
https://clinicaltrials.gov/show/NCT00685581
Palavras-chave
Versões (1)
- 12/07/2017 12/07/2017 -
Transferido a
12 de julho de 2017
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Cardiovascular Disease NCT00685581
Eligibility Cardiovascular Disease NCT00685581
- StudyEvent: Eligibility
Similar models
Eligibility Cardiovascular Disease NCT00685581
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
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])
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])
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])
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])
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])
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])
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])
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])
C0015737 (UMLS CUI [1,2])
C0242193 (UMLS CUI [1,3])
C0030705 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])