This is a multicenter, randomized, double-blind, placebo-controlled trial to investigate the clinical efficacy of treatment with exogenous dietary ketone supplement containing 1,3-butanediol in patients hospitalized with acute heart failure (AHF), potentially leading to better clinical outcomes.
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Change in clinical benefit during 1,3-butanediol treatment versus placebo
Timeframe: From baseline (day 0) to end of treatment (day 30)