Outpatients | Age
Item
male and female outpatients 18 years of age and older
boolean
C0029921 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
Antihypertensive Agents | Diastolic blood pressure | Antihypertensive Agents Absent
Item
patients with antihypertensive agents at screening: dbp<110mmhg or patients without antihypertensive agents at screening: dbp 90mmhg~120mmhg
boolean
C0003364 (UMLS CUI [1])
C0428883 (UMLS CUI [2])
C0003364 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Informed Consent
Item
subjects who agree to participate in this sudy and give written informed consent
boolean
C0021430 (UMLS CUI [1])
Comprehension Study Protocol | Cooperative Behavior | Follow-up Able
Item
subjects considered to understand the study, be cooperative, and able to be followed-up until the end of the study
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0009964 (UMLS CUI [2])
C3274571 (UMLS CUI [3,1])
C0085732 (UMLS CUI [3,2])
Blood Pressure Uncontrolled | Fimasartan Dose | Diastolic blood pressure | Systolic Pressure
Item
patients with not controlled blood pressure at baseline visit, by fimasartan 60mg 4weeks treatment, dbp 90mmhg~109mmhg and sbp<180mmhg
boolean
C0005823 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C2825622 (UMLS CUI [2,1])
C0178602 (UMLS CUI [2,2])
C0428883 (UMLS CUI [3])
C0871470 (UMLS CUI [4])
Sitting diastolic blood pressure | Severe Hypertension Sitting systolic blood pressure | Secondary hypertension
Item
the sitting dbp is more than 120mmhg or severe hypertensive patient with sitting systolic blood pressure over 200mmhg patients with secondary hypertension
boolean
C1319894 (UMLS CUI [1])
C4013784 (UMLS CUI [2,1])
C1319893 (UMLS CUI [2,2])
C0155616 (UMLS CUI [3])
Mean blood pressure Difference mean | Sitting diastolic blood pressure | Sitting systolic blood pressure
Item
patients who are measured the mean difference of mean blood pressure under sidbp 10mmhg or sisbp 20mmhg at screening or baseline visit
boolean
C0428886 (UMLS CUI [1,1])
C1705242 (UMLS CUI [1,2])
C0444504 (UMLS CUI [1,3])
C1319894 (UMLS CUI [2])
C1319893 (UMLS CUI [3])
Kidney Disease Severe | Serum creatinine raised | Gastrointestinal Disease Severe | Hematological Disease Severe | Liver disease Severe | Aspartate aminotransferase increased | Alanine aminotransferase increased | Disease Affecting Drug absorption | Disease Affecting Drug disposition | Disease Affecting Drug metabolism | Disease Affecting Drug elimination
Item
patients with severe renal(creatinine more 1.5 times than upper limit of normal), gastrointestinal, hematological or hepatic(ast, alt more 2 twice more than upper limit of normal)disease etc. which might affect absorption, disposition, metabolism or excretion of the drug
boolean
C0022658 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0700225 (UMLS CUI [2])
C0017178 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0018939 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C0023895 (UMLS CUI [5,1])
C0205082 (UMLS CUI [5,2])
C0151904 (UMLS CUI [6])
C0151905 (UMLS CUI [7])
C0012634 (UMLS CUI [8,1])
C0392760 (UMLS CUI [8,2])
C0678745 (UMLS CUI [8,3])
C0012634 (UMLS CUI [9,1])
C0392760 (UMLS CUI [9,2])
C0678755 (UMLS CUI [9,3])
C0012634 (UMLS CUI [10,1])
C0392760 (UMLS CUI [10,2])
C0683140 (UMLS CUI [10,3])
C0012634 (UMLS CUI [11,1])
C0392760 (UMLS CUI [11,2])
C0683141 (UMLS CUI [11,3])
Hypotension, Orthostatic
Item
patients with postural hypotension
boolean
C0020651 (UMLS CUI [1])
Insulin-Dependent Diabetes Mellitus Severe | Diabetic - poor control | Hemoglobin A1c measurement | Therapy change Oral hypoglycemic | Insulin regime Before Screening
Item
patients with sever insulin dependent diabetes mellitus or uncontrolled diabetes mellitus(hba1c>9%, regimen change of oral hypoglycemic agents within 12weeks, treated insulin before screening)
boolean
C0011854 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0421258 (UMLS CUI [2])
C0474680 (UMLS CUI [3])
C3665894 (UMLS CUI [4,1])
C0359086 (UMLS CUI [4,2])
C0557978 (UMLS CUI [5,1])
C0332152 (UMLS CUI [5,2])
C0220908 (UMLS CUI [5,3])
Myocardial Infarction | Coronary Artery Disease Severe | Heart failure | Valvular defects
Item
patients with a history of myocardial infarction, severe coronary artery disease or clinically significant heart failure or valvular defect in last 6 months
boolean
C0027051 (UMLS CUI [1])
C1956346 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0018801 (UMLS CUI [3])
C2748945 (UMLS CUI [4])
Phthisis | Autoimmune Disease | Connective Tissue Disease
Item
patients with consumptive disease, autoimmune disease, connective tissue disease
boolean
C0041327 (UMLS CUI [1])
C0004364 (UMLS CUI [2])
C0009782 (UMLS CUI [3])
Hepatitis B | Hepatitis C | Hepatitis B carrier | Hepatitis C carrier
Item
patients with a history of type b or c hepatitis(include carrier)
boolean
C0019163 (UMLS CUI [1])
C0019196 (UMLS CUI [2])
C0262505 (UMLS CUI [3])
C0400920 (UMLS CUI [4])
HIV Infection | Hepatitis
Item
patients with hiv or hepatitis
boolean
C0019693 (UMLS CUI [1])
C0019158 (UMLS CUI [2])
Laboratory test result abnormal
Item
patients with clinically significant laboratory abnormality
boolean
C0438215 (UMLS CUI [1])
Pharmaceutical Preparations Affecting Blood Pressure | Therapeutic procedure Influence Blood Pressure
Item
patients receiving any drugs known to affect blood pressure or medical treatments that can influence the blood pressure
boolean
C0013227 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0005823 (UMLS CUI [1,3])
C0087111 (UMLS CUI [2,1])
C4054723 (UMLS CUI [2,2])
C0005823 (UMLS CUI [2,3])
Allergy to angiotensin II receptor antagonist | Medical contraindication Angiotensin II receptor antagonist
Item
patients with allergy or contraindication to any angiotensin ii receptor antagonists
boolean
C2585204 (UMLS CUI [1])
C1301624 (UMLS CUI [2,1])
C0521942 (UMLS CUI [2,2])
Childbearing Potential Hysterectomy Absent | Childbearing Potential Postmenopausal state Absent
Item
female of childbearing potential who does not undergo hysterectomy or is not post-menopausal
boolean
C3831118 (UMLS CUI [1,1])
C0020699 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C3831118 (UMLS CUI [2,1])
C0232970 (UMLS CUI [2,2])
C0332197 (UMLS CUI [2,3])
Substance Use Disorders
Item
patients judged to have a history of alcohol or drug abuse by the investigator
boolean
C0038586 (UMLS CUI [1])
Study Subject Participation Status | Clinical Trial | Study Subject Participation Status Inappropriate
Item
patients participated other clinical trial 12 weeks before screening - patients judged to be inappropriate for this study by the investigator with other reasons
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2])
C2348568 (UMLS CUI [3,1])
C1548788 (UMLS CUI [3,2])