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. 2021 Jan 12;11:569132. doi: 10.3389/fphar.2020.569132

TABLE 1.

Randomized controlled study of trimetazidine in heart failure.

year study patients (T/c) NISH ISH LVEF TMZ (mg/d) Time LVEF* other endpoints Positive/none
2004 Thrainsdottir et al. (2004) 10/9 50% 50% <40% 60 1 month 33 ± 8% vs. 37 ± 16% / none
2006 Fragasso et al. (2006b) 12/12 / / <45% 60 90 days 34 ± 10% vs. 39 ± 10% PCr / ATP: 1.80 ± 0.50 vs. 1.35 ± 0.33 none
2006 Fragasso et al. (2006a) 28/27 / 100% <45% 60 13 months 43 ± 10% vs. 34 ± 7% / postive
2007 Di Napoli et al. (2007) 30/31 34.40% 100% <35% 60 48 months ∼40% vs. ∼30% / positive
2008 Tuunanen et al. (2008) 12/7 / 100% <40% 70 3 months 34.8 ± 12% vs. 31.9 ± 12% / positive
2009 Gunes et al. (2009a) 51/35 29% 66% <40% 60 3 months 42.4% ± 6.3% vs. 33.2% ± 6.6% / positive
2009 Gunes et al. (2009b) 36/36 / 33% <40% 60 6 months 32.7 ± 6.5% vs. 37.2 ± 5.5% Max P-wave duration :106.7 ± 15.8 vs. 91.7 ± 12.7 ms none
2010 Cera et al. (2010) 17/13 / 60% <45% 60 6 months 40.11 ± 1.23% vs. 37.97 ± 13.21%; QTc interval duration: 451.81 ± 55.02 vs. 453.20 ± 51.50 positive
2011 Fragasso et al. (2011) 25/19 34% 66% <45% 60 36 months 42 ± 11% vs.36 ± 6% REE: 1,580 ± 263 vs. 1,690 ± 337 kcal/day positive
2014 Winter et al. (2014) 30/30 100% 0 <45% 70 6 months 31 ± 10% vs. 34 ± 8% 6MWT: 443 ±25 vs. 506 ±79 m; (18) FDG-PET SUV: 7.0 ±3.6 vs. 8.2±3.4 none
2016 Momen et al. (2016) 55/53 / 100% <40% 70 6 months 36.6% vs. 31.2% / positive
2016 Jatain et al. (2016) 52/48 46% / <45% 60 3 months 30.9% vs 27% 6MWT: 402 vs. 349.7 m positive

T/c, TMZ/control, trimetazdine group/control group; NISH, non ischemic heart disease; ISH, ischemic heart disease; LVEF, left ventricular ejection fraction stated in the inclusion criteria of the clinical trial, LVEF represents the fact that all patients included in the study had an LVEF < the number indicated; LVEF *, the average LVEF of all patients after treatment, trimetazdine group vs. control group; TMZ, trimetazidine; 6MWT, 6 min walk test; REE, Whole body resting energy expenditure; FDG-PET, β-2-[18 F]-Fluoro-2-deoxy-D-glucose-Positron Emission Tomography; PCr/ATP, phosphocreatine/adenosine triphosphate.