Age
Item
patients aged between 18 and 75
boolean
C0001779 (UMLS CUI [1])
Essential Hypertension | Sitting diastolic blood pressure
Item
patients with essential hypertension {95 mmhg ≤ sitdbp< 115 mmhg at the end of placebo run-in treatment period}
boolean
C0085580 (UMLS CUI [1])
C1319894 (UMLS CUI [2])
Sitting systolic blood pressure mean
Item
patients with mean sitsbp ≥ 200 mmhg
boolean
C1319893 (UMLS CUI [1,1])
C0444504 (UMLS CUI [1,2])
Hypersensitivity Dihydropyridines | Allergy to angiotensin II receptor antagonist
Item
patients with known hypersensitivity to dihydropyridine or angiotensin ii receptor blockers
boolean
C0020517 (UMLS CUI [1,1])
C0012315 (UMLS CUI [1,2])
C2585204 (UMLS CUI [2])
Secondary hypertension | Secondary hypertension Suspected
Item
patients with secondary hypertension or suspected secondary hypertension
boolean
C0155616 (UMLS CUI [1])
C0155616 (UMLS CUI [2,1])
C0750491 (UMLS CUI [2,2])
Malignant Hypertension
Item
patients with malignant hypertension
boolean
C0020540 (UMLS CUI [1])
Pharmaceutical Preparations Interactions Possible Investigational New Drugs
Item
patients who have received any medications with possible interactions with study drugs
boolean
C0013227 (UMLS CUI [1,1])
C0687133 (UMLS CUI [1,2])
C0332149 (UMLS CUI [1,3])
C0013230 (UMLS CUI [1,4])
Diabetic - poor control
Item
patients with uncontrolled diabetes
boolean
C0421258 (UMLS CUI [1])
Heart Disease Severe | Cerebrovascular Disorder Severe
Item
patients with severe heart disease or severe cerebrovascular disease
boolean
C0018799 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0007820 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
Test Result Hematologic Clinical Significance | Kidney Disease | Creatinine measurement, serum | Liver disease | Alanine aminotransferase measurement | Aspartate aminotransferase measurement
Item
patients with clinically significant hematological test results, renal disease (serum creatinine) or liver disease (alt or ast)
boolean
C0456984 (UMLS CUI [1,1])
C0205488 (UMLS CUI [1,2])
C2826293 (UMLS CUI [1,3])
C0022658 (UMLS CUI [2])
C0201976 (UMLS CUI [3])
C0023895 (UMLS CUI [4])
C0201836 (UMLS CUI [5])
C0201899 (UMLS CUI [6])
Malignant disease
Item
patients with a history of malignant disease
boolean
C0442867 (UMLS CUI [1])
Autoimmune Disease
Item
patients with a history of autoimmune disease
boolean
C0004364 (UMLS CUI [1])
Pregnancy test positive | Breast Feeding | Pregnancy, Planned
Item
women with a positive pregnancy test result, breast feeding or intention of pregnancy during the trial
boolean
C0240802 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
Other Reason Study Subject Participation Status Inappropriate
Item
patients inappropriate to be included in study population due to other reasons at the discretion of the investigator
boolean
C3840932 (UMLS CUI [1,1])
C2348568 (UMLS CUI [1,2])
C1548788 (UMLS CUI [1,3])