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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.
4                                              Trandolapril and hydrochlorothiazide were used as added
5                                              Trandolapril and/or hydrochlorothiazide was administered
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
8                                The verapamil-trandolapril-based strategy was as clinically effective
9 nificantly after 12 months of treatment with trandolapril compared with placebo.
10                                     Although trandolapril did not improve survival in the overall PEA
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
14                            The ACE inhibitor trandolapril may improve peripheral neuropathy in normot
15 ons between hs-CRP levels and the effects of trandolapril on any of the above outcomes.
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
21                                              Trandolapril significantly reduced the risk of cardiovas
22                  The INternational VErapamil-trandolapril STudy (INVEST) compared outcomes in hyperte
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
26 rticipants in the International Verapamil SR-Trandolapril Study (INVEST).
27 lapril in INVEST (INternational VErapamil SR Trandolapril STudy) were categorized into 3 groups on th
28 s (n=8290) were randomly assigned to receive trandolapril (target, 4 mg/d) or placebo.
29                                The effect of trandolapril therapy on outcomes was not modified signif
30                                Nevertheless, trandolapril therapy was associated with a significantly
31           Lower follow-up BP and addition of trandolapril to verapamil SR each were associated with r
32                                              Trandolapril was also recommended for patients with hear
33                                              Trandolapril was associated with a reduction in total mo
34 r blockade (candesartan) and ACE inhibition (trandolapril) were also tested in LTM.
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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