Age
Item
males and females who are at least 18 years of age at time of enrollment
boolean
C0001779 (UMLS CUI [1])
Informed Consent
Item
subject understands the investigational nature of the study and provides written, informed consent.
boolean
C0021430 (UMLS CUI [1])
Lipid Modification Therapy | Statins | Fibrates | Bile acid sequestrants
Item
subjects taking any lipid modification therapy, including but not limited to statins, fibrates and bile acid sequestrants.
boolean
C0023779 (UMLS CUI [1,1])
C3840684 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C0360714 (UMLS CUI [2])
C1449704 (UMLS CUI [3])
C2917337 (UMLS CUI [4])
Fish Oil Interferes with Clinical Trial | Supplements Interfere with Clinical Trial
Item
subjects taking fish oil or any other supplements, which in the investigator s opinion may interfere with the study.
boolean
C0016157 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0242295 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0008976 (UMLS CUI [2,3])
Liver disease | Peptic Ulcer
Item
subjects with acute liver disease or active peptic ulcer disease.
boolean
C0023895 (UMLS CUI [1])
C0030920 (UMLS CUI [2])
Increased uric acid level | Gout
Item
subjects with elevated uric acid levels or gout
boolean
C0041981 (UMLS CUI [1])
C0018099 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnancy or women currently breastfeeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Gender Hormonal Contraceptives | Gender Hormone replacement therapy
Item
female subjects taking hormonal contraceptives or hormone replacement therapy may be included in this study only if they have been on a stable dose for at least 3 months.
boolean
C0079399 (UMLS CUI [1,1])
C0009907 (UMLS CUI [1,2])
C0079399 (UMLS CUI [2,1])
C0282402 (UMLS CUI [2,2])
Body mass index
Item
bmi less than 18.5
boolean
C1305855 (UMLS CUI [1])
Body Weight Variation Percentage Timespan
Item
subjects with weight that varies greater than 20% over the past 3 months.
boolean
C0005910 (UMLS CUI [1,1])
C0205419 (UMLS CUI [1,2])
C0439165 (UMLS CUI [1,3])
C0872291 (UMLS CUI [1,4])
Pharmaceutical Preparations Interfere with Clinical Trial | Bile acid sequestrants | Antibiotics | Anticoagulants | Anticonvulsants | Anti-Arrhythmia Agents | Cyclosporine | MYCOPHENOLATE | Synthroid | Chronic diarrhea | Gastric Bypass | Gastric band | Ostomy | Motility disorder of intestine | Condition Affecting Intestinal fat absorption
Item
subjects taking the following medications for at least six weeks, which may interfere with the study, will be excluded: bas, antibiotics, anticoagulants, anticonvulsants, antiarrhythmic, cyclosporine, mycophenolate and synthroid. subjects with chronic diarrhea, gastric bypass or lap band procedures, ostomies, bowel motility problems, or other conditions that could affect intestinal fat absorption.
boolean
C0013227 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C2917337 (UMLS CUI [2])
C0003232 (UMLS CUI [3])
C0003280 (UMLS CUI [4])
C0003286 (UMLS CUI [5])
C0003195 (UMLS CUI [6])
C0010592 (UMLS CUI [7])
C0883242 (UMLS CUI [8])
C0728762 (UMLS CUI [9])
C0401151 (UMLS CUI [10])
C0017125 (UMLS CUI [11])
C1960832 (UMLS CUI [12])
C0029473 (UMLS CUI [13])
C0400865 (UMLS CUI [14])
C0348080 (UMLS CUI [15,1])
C0392760 (UMLS CUI [15,2])
C0232653 (UMLS CUI [15,3])
Pharmaceutical Preparations New | Pharmaceutical Preparations Multiple
Item
subjects initiating new medications or patients on multiple medications may also be excluded.
boolean
C0013227 (UMLS CUI [1,1])
C0205314 (UMLS CUI [1,2])
C0013227 (UMLS CUI [2,1])
C0439064 (UMLS CUI [2,2])
Lacking Able to swallow Capsule
Item
inability to swallow capsules
boolean
C0332268 (UMLS CUI [1,1])
C2712086 (UMLS CUI [1,2])
C0006935 (UMLS CUI [1,3])
Diabetes Mellitus, Insulin-Dependent | Diabetes Mellitus, Non-Insulin-Dependent | Hemoglobin A1c measurement
Item
patients with a history of type i or type ii diabetes or hba1c greater than 6.5%.
boolean
C0011854 (UMLS CUI [1])
C0011860 (UMLS CUI [2])
C0474680 (UMLS CUI [3])
Condition Interferes with Research results | Disease Interferes with Research results | Condition At risk Patient safety | Disease At risk Patient safety
Item
volunteers may also be excluded, if in the opinion of the study investigators, they have some other condition or disorder that may adversely affect the outcome of the study or the safety of the volunteer.
boolean
C0348080 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0683954 (UMLS CUI [1,3])
C0012634 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0683954 (UMLS CUI [2,3])
C0348080 (UMLS CUI [3,1])
C1444641 (UMLS CUI [3,2])
C1113679 (UMLS CUI [3,3])
C0012634 (UMLS CUI [4,1])
C1444641 (UMLS CUI [4,2])
C1113679 (UMLS CUI [4,3])