Age | Gender Healthy
Item
age between 19 to 45, healthy male subjects(at screening)
boolean
C0001779 (UMLS CUI [1])
C0079399 (UMLS CUI [2,1])
C3898900 (UMLS CUI [2,2])
Body Weight | Body mass index
Item
body weight between 55kg - 90kg, bmi between 18.0 - 27.0
boolean
C0005910 (UMLS CUI [1])
C1305855 (UMLS CUI [2])
Plasma fasting glucose measurement
Item
fpg 60-125mg/dl glucose level(at screening)
boolean
C0583513 (UMLS CUI [1])
Comprehension Clinical Trial | Informed Consent
Item
volunteer who totally understands the progress of this clinical trials, make decision by his free will, and signed a consent form to follow the progress.
boolean
C0162340 (UMLS CUI [1,1])
C0008976 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2])
Liver disease | Carrier of viral hepatitis | Kidney Disease | Nervous system disorder | Immune System Disease | Lung disease | Endocrine System Disease | Hematologic Neoplasm | Heart Disease | Mental disorder
Item
volunteer who has past or present history of any diseases following below.(liver including hepatitis virus carrier, kidney, neurology, immunology, pulmonary, endocrine, hematooncology, cardiology, mental disorder)
boolean
C0023895 (UMLS CUI [1])
C0733680 (UMLS CUI [2])
C0022658 (UMLS CUI [3])
C0027765 (UMLS CUI [4])
C0021053 (UMLS CUI [5])
C0024115 (UMLS CUI [6])
C0014130 (UMLS CUI [7])
C0376545 (UMLS CUI [8])
C0018799 (UMLS CUI [9])
C0004936 (UMLS CUI [10])
Gastrointestinal Disease | Crohn Disease | Ulcer | Pancreatitis | Pancreatitis, Chronic | Gastrointestinal Surgical Procedure | Exception Appendectomy | Exception Hernioplasty
Item
volunteer who had gi tract disease(crohn's disease, ulcer, acute or chronic pancreatitis) or surgery(appendectomy, hernioplasty are excluded)
boolean
C0017178 (UMLS CUI [1])
C0010346 (UMLS CUI [2])
C0041582 (UMLS CUI [3])
C0030305 (UMLS CUI [4])
C0149521 (UMLS CUI [5])
C0524722 (UMLS CUI [6])
C1705847 (UMLS CUI [7,1])
C0003611 (UMLS CUI [7,2])
C1705847 (UMLS CUI [8,1])
C0019328 (UMLS CUI [8,2])
Aspirin allergy | Allergic reaction to antibiotics
Item
volunteer who had drug(aspirin, antibiotics) hypersensitivity reaction
boolean
C0004058 (UMLS CUI [1])
C0850093 (UMLS CUI [2])
Study Subject Participation Status
Item
subject who already participated in other trials in 2 months
boolean
C2348568 (UMLS CUI [1])
Blood Donation Whole | Blood Donation Component | Blood Transfusion
Item
subject who had whole blood donation in 2 months, or component blood donation in 1 months or transfusion
boolean
C0005794 (UMLS CUI [1,1])
C0439751 (UMLS CUI [1,2])
C0005794 (UMLS CUI [2,1])
C1705248 (UMLS CUI [2,2])
C0005841 (UMLS CUI [3])