Valsartan in Cardiovascular Disease With Renal Dysfunction (The V-CARD) Study
Hypertension
About this trial
This is an interventional prevention trial for Hypertension focused on measuring Cardiorenal syndrome, Renal dysfunction, Cardiovascular events, Valsartan
Eligibility Criteria
Inclusion Criteria (all required): Systolic blood pressure (SBP) >/= 140 and/or diastolic blood pressure (DBP) >/= 90 (untreated hypertension cases); or SBP>/=130 and/or DBP>/=80 (treated hypertension cases) Patients with coronary artery disease (more than 50% stenosis on coronary angiography [CAG], coronary computed tomography [CT] or coronary magnetic resonance angiography [MRA]; coronary spasm; or history of percutaneous coronary intervention [PCI]);Unstable angina patient Creatinine clearance between 30.0 and 89.9 ml/min Exclusion Criteria (at least one of following): Reduced left ventricular (LV) function (ejection fraction [EF] equal to or less than 40%) Hyperpotassemia (serum potassium equal to or more than 5.5 mEq/l) Rapid progressive glomerular nephritis Nephrotic syndrome Renal artery stenosis Uncontrolled diabetes (HbA1c equal to or more than 9.0%) History of allergy to valsartan Pregnant women
Sites / Locations
- Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University
- Department of Cardiovascular Medicine, Kumamoto University Hospital
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Valsartan 40mg
Valsartan 160mg
Standard Dose valsartan
High Dose valsartan