Clinical Trial

Ketone Ester for Treatment Of Acute Heart Failure

Study acronym: KETO-AHF
Not Yet Recruiting
View on ClinicalTrials.gov →
Summary
Ketones have been suggested to have significant physiological effects in patients with heart failure. Potential mechanisms for these effects include energy provision for the failing heart and direct protective effects on other organs. Despite the strong physiological rationale, the acute effects of ketone therapy in patients with acute heart failure (AHF) is unclear. AHF is a major healthcare issue, with in-hospital mortality exceeding 10%. Therefore, we propose a vanguard randomized controlled trial to assess the effects of ketone esters in patients with AHF. Sixty patients hospitalized with AHF will be randomized to receive either 25 grams of ketone esters three times per day or a matching placebo for five days, or until death or hospital discharge. We hypothesize that ketone therapy will improve markers of systemic congestion and heart failure symptoms. Primary endpoint will be changes in NT-proBNP levels during therapy. Secondary endpoints will be KCCQ scores, and hemodynamic profile as assessed by echocardiogram. Exploratory endpoints will clinical outcomes including mortality, need for intensive care unit admission, among others.
Protocol Amendment History 1 change
notable Primary completion pushed: 2027-03 -> 2027-07 2026-06-05
Trial Details
NCT Number NCT07434466
Lead Sponsor University of Alberta
Collaborators: Canadian VIGOUR Centre, University Hospital Foundation
Conditions Acute Heart Failure
Enrollment 60 participants
Start Date 2026-09
Primary Completion 2027-07 (estimated)
Study Completion 2028-03 (estimated)
Updated on ClinicalTrials.gov 2026-08-13