Informatie:
Fout:
ID
27649
Beschrijving
Impact of a Nutritional Supplement on Metabolic Health; ODM derived from: https://clinicaltrials.gov/show/NCT02239198
Link
https://clinicaltrials.gov/show/NCT02239198
Trefwoorden
Versies (1)
- 24-11-17 24-11-17 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
24 november 2017
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Cardiovascular Disease Prevention NCT02239198
Eligibility Cardiovascular Disease Prevention NCT02239198
- StudyEvent: Eligibility
Similar models
Eligibility Cardiovascular Disease Prevention NCT02239198
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
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])
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])
C0013227 (UMLS CUI [2,1])
C0428896 (UMLS CUI [2,2])
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])
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])
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])
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])
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])
C3831118 (UMLS CUI [2,1])
C0430057 (UMLS CUI [2,2])