Gender
Item
male or female
boolean
C0079399 (UMLS CUI [1])
Age
Item
aged 20 to 80 years old.
boolean
C0001779 (UMLS CUI [1])
Adult | Essential Hypertension Untreated | Essential Hypertension Treated Uncontrolled
Item
adult with essential hypertension - either newly diagnosed and untreated, or previously treated and uncontrolled
boolean
C0001675 (UMLS CUI [1])
C0085580 (UMLS CUI [2,1])
C0332155 (UMLS CUI [2,2])
C0085580 (UMLS CUI [3,1])
C1522326 (UMLS CUI [3,2])
C0205318 (UMLS CUI [3,3])
Sitting systolic blood pressure | Sitting diastolic blood pressure
Item
sitting blood pressure: systolic bp > 140 mmhg but < 180 mmhg, and/or diastolic bp > 90 mmhg but < 110 mmhg)
boolean
C1319893 (UMLS CUI [1])
C1319894 (UMLS CUI [2])
Cardiovascular risk factor Quantity | Exception Hypertensive disease | Diabetes Mellitus | Hyperglycemia | Cholesterol | Dyslipidemias | Cardiovascular event | Target Organ Damage | Family history of Hypertension | Family history of Cardiovascular disease | Age | Gender | Tobacco use | Overweight | Obesity
Item
at least one cardiovascular known risk factor other than hypertension: diabetes/hyperglycaemia, cholesterol /dyslipidemia, a previous cardiovascular event, target organ damage, family history of hypertension or cardiovascular diseases, old age defined as > 55 years (males), > 65 years (females), smoking, overweight or obese patients or a combination of above risk factors
boolean
C0850624 (UMLS CUI [1,1])
C1265611 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0020538 (UMLS CUI [2,2])
C0011849 (UMLS CUI [3])
C0020456 (UMLS CUI [4])
C0008377 (UMLS CUI [5])
C0242339 (UMLS CUI [6])
C1320716 (UMLS CUI [7])
C1521840 (UMLS CUI [8,1])
C0178784 (UMLS CUI [8,2])
C0010957 (UMLS CUI [8,3])
C0455405 (UMLS CUI [9])
C0455404 (UMLS CUI [10])
C0001779 (UMLS CUI [11])
C0079399 (UMLS CUI [12])
C0543414 (UMLS CUI [13])
C0497406 (UMLS CUI [14])
C0028754 (UMLS CUI [15])
Patients Benefit Angiotensin II receptor antagonist
Item
patients who are assessed to benefit from the intake of angiotensin ii receptor blocker (arb) monotherapy or as add-on medication
boolean
C0030705 (UMLS CUI [1,1])
C0814225 (UMLS CUI [1,2])
C0521942 (UMLS CUI [1,3])
Medical contraindication Telmisartan
Item
patients with contraindications to telmisartan use (as per the micardis® tablets package insert).
boolean
C1301624 (UMLS CUI [1,1])
C0248719 (UMLS CUI [1,2])
Hypersensitivity Ingredient Micardis | Hypersensitivity Excipient Micardis
Item
known hypersensitivity to the active ingredient or to any of the excipients of micardis® .
boolean
C0020517 (UMLS CUI [1,1])
C1550600 (UMLS CUI [1,2])
C0721704 (UMLS CUI [1,3])
C0020517 (UMLS CUI [2,1])
C0015237 (UMLS CUI [2,2])
C0721704 (UMLS CUI [2,3])
Other medical condition Investigational New Drugs At risk
Item
any other clinical condition which, in the opinion of the attending physician, would not allow safe administration of the study medications.
boolean
C3843040 (UMLS CUI [1,1])
C0013230 (UMLS CUI [1,2])
C1444641 (UMLS CUI [1,3])
Study Subject Participation Status | Clinical Trial
Item
patients participating in any other clinical trial.
boolean
C2348568 (UMLS CUI [1])
C0008976 (UMLS CUI [2])
Micardis Pre-existing | Micardis Combination Pre-existing
Item
patients already on micardis® alone or combination
boolean
C0721704 (UMLS CUI [1,1])
C2347662 (UMLS CUI [1,2])
C0721704 (UMLS CUI [2,1])
C0205195 (UMLS CUI [2,2])
C2347662 (UMLS CUI [2,3])
Pregnancy | Breast Feeding
Item
pregnant females, or females breast feeding.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])