The traditional Chinese medicine Qiliqiangxin in heart failure with reduced ejection fraction: a randomized, double-blind, placebo-controlled trial.
Iokfai CheangWenming YaoYanli ZhouXu ZhuGehui NiXinyi LuShengen LiaoRongrong GaoFang ZhouJiangang ShenAlice Yeuk Lan LeungMeng JiangHong KongLing BaiAiliman MahemutiHaitao YuanYu-Gang DongChun-Ka WongQinghua XuGaoxing ZhangJianhua WuQi LuJunhai ZhangChunxi ChaQian RenLu FuBing WangYongshun XuHouxiang HuJing DongZhuo ShangChaoping YuSongsen LiChen YaoLingling GaoHaifeng ZhangAnthony RosenzweigZhen-Hua JiaXinli Linull nullPublished in: Nature medicine (2024)
Previous findings have indicated the potential benefits of the Chinese traditional medicine Qiliqiangxin (QLQX) in heart failure. Here we performed a double-blind, randomized controlled trial to evaluate the efficacy and safety of QLQX in patients with heart failure and reduced ejection fraction (HFrEF). This multicenter trial, conducted in 133 hospitals in China, enrolled 3,110 patients with HFrEF with NT-proBNP levels of ≥450 pg ml -1 and left ventricular ejection fraction of ≤40%. Participants were randomized to receive either QLQX capsules or placebo (four capsules three times daily) alongside standard heart failure therapy. The trial met its primary outcome, which was a composite of hospitalization for heart failure and cardiovascular death: over a median follow-up of 18.3 months, the primary outcome occurred in 389 patients (25.02%) in the QLQX group and 467 patients (30.03%) in the placebo group (hazard ratio (HR), 0.78; 95% confidence interval (CI), 0.68-0.90; P < 0.001). In an analysis of secondary outcomes, the QLQX group showed reductions in both hospitalization for heart failure (15.63% versus 19.16%; HR, 0.76; 95% CI, 0.64-0.90; P = 0.002) and cardiovascular death (13.31% versus 15.95%; HR, 0.83; 95% CI, 0.68-0.996; P = 0.045) compared to the placebo group. All-cause mortality did not differ significantly between the two groups (HR, 0.84; 95% CI, 0.70-1.01; P = 0.058) and adverse events were also comparable between the groups. The results of this trial indicate that QLQX may improve clinical outcomes in patients with HFrEF when added to conventional therapy. ChiCTR registration: ChiCTR1900021929 .
Keyphrases
- heart failure
- double blind
- ejection fraction
- phase iii
- placebo controlled
- study protocol
- left ventricular
- clinical trial
- phase ii
- aortic stenosis
- randomized controlled trial
- end stage renal disease
- open label
- cardiac resynchronization therapy
- newly diagnosed
- healthcare
- acute heart failure
- peritoneal dialysis
- prognostic factors
- cross sectional
- climate change
- risk assessment
- bone marrow
- physical activity
- adipose tissue
- left atrial