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   1  the angiotensin-converting enzyme inhibitor trandolapril.                                           
     2 chlorothiazide; and 4113 (52.4%) were taking trandolapril.                                           
     3 concise enantioselective formal synthesis of trandolapril.                                           
  
  
     6  sustained release; 4934 (62.9%) were taking trandolapril; and 3430 (43.7%) were taking hydrochloroth
     7 nts were randomly assigned to receive either trandolapril at a target dose of 4 mg per day (4158 pati
  
  
  
    11 nt in the placebo group (hazard ratio in the trandolapril group, 0.96; 95 percent confidence interval
    12 y revascularization--was 21.9 percent in the trandolapril group, as compared with 22.5 percent in the
    13 thiazide or verapamil-SR (sustained release)/trandolapril in INVEST (INternational VErapamil SR Trand
  
  
    16 eserved systolic function were randomized to trandolapril or placebo and followed up for a median of 
    17 lar ejection fraction who were randomized to trandolapril or placebo as part of the Prevention of Eve
    18 ,627 patients with SIHD randomly assigned to trandolapril or placebo within the PEACE (Prevention of 
    19 ort, in which mean eGFR was relatively high, trandolapril reduced mortality in patients with reduced 
    20 tients in the top quartile of FGF-23 levels, trandolapril significantly reduced cardiovascular death 
  
  
    23 0 patients of the International Verapamil SR/Trandolapril Study (INVEST) Genetic Substudy (INVEST-GEN
    24  objective of the International Verapamil SR/Trandolapril Study (INVEST) is to compare the risk for a
    25 sis of data from the International Verapamil-Trandolapril Study (INVEST), which was conducted from Se
  
    27 lapril in INVEST (INternational VErapamil SR Trandolapril STudy) were categorized into 3 groups on th
  
  
  
  
  
  
  
    35 0 mm Hg (HRs 0.82 or 0.70, respectively) and trandolapril with verapamil SR (HRs 0.78 and 0.79) were 
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