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✓ Translated by DotMD AI Clinical Council Source: Vnitrni lekarstvi • Phase III Randomized Trial
Verify Primary Source: NIH PubMed PMID #34171959 ↗

Phase III Randomized Trial: [Vericiguat in patients with heart failure and reduced ejection fraction] (N = 691)

Original Paper Title: “[Vericiguat in patients with heart failure and reduced ejection fraction]”

Elena Rostova (AI Quant) Rigor Score
93 / 100
Sample Size (Participants)
N = 691
Evidence Classification
Phase III Randomized Trial
Sarah Jenkins, RN (AI Plain-English Editor) • Key Takeaways
  • Among patients with high-risk heart failure, the incidence of death from cardiovascular causes or hospitalization for heart failure was lower among those who received vericiguat than those who received placebo.
  • Study Design & Sample: Phase III Randomized Trial published in Vnitrni lekarstvi (N = 691 human participants).
  • Biostatistical Rigor Score: 93/100 audited by Elena Rostova (AI Biostatistician & openFDA Quant).

What the Study Found (In Plain English)

Published in Vnitrni lekarstvi (2021), this phase iii randomized trial evaluating 691 human participants investigated: The effect of vericiguat, a novel oral soluble guanylate cyclase stimulator, in patients with heart failure and reduced ejection fraction who had recently been hospitalized or had received intravenous diuretic therapy is unclear. Key clinical takeaway: Among patients with high-risk heart failure, the incidence of death from cardiovascular causes or hospitalization for heart failure was lower among those who received vericiguat than those who received placebo.

Dr. Lin (AI Evidence Lead): Statistical Endpoints & Numbers

Primary Endpoint & Quantitative Summary (Vnitrni lekarstvi, 2021-01-15; N = 691; Rigor 93/100): Among patients with high-risk heart failure, the incidence of death from cardiovascular causes or hospitalization for heart failure was lower among those who received vericiguat than those who received placebo.

Study Limitations & Caveats Before You Act

Clinical trials evaluate specific inclusion/exclusion cohorts under protocol-controlled conditions (Phase III Randomized Trial). Individual response, hepatic/renal clearance, CYP450 drug interactions, and baseline comorbidities vary; verify applicability with a board-certified physician before modifying any prescription or supplement regimen.

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