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Acute Oral Ketones or Carbohydrate Supplement Modify Heart Function in Heart Failure?

Does Oral Intake of Beta-hydroxybutyrate Decrease Left Ventricular End-systolic Volume at Cardiac Magnetic Resonance in Patients With Heart Failure Compared to Carbohydrate Placebo?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05651529
Enrollment
20
Registered
2022-12-15
Start date
2022-12-16
Completion date
2025-12-16
Last updated
2026-01-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

Ketones, Heart

Brief summary

Does oral intake of exogenous ketone salt improve heart function measured by cardiac MRI in heart failure compared to oral intake of a carbohydrate placebo?

Detailed description

This study will help to quantify heart and kidney ketone uptake with or without an exogenous ketone salt in heart failure condition. Participants will have 2 different cardiac MRI to perform: 1. Fasting with exogenous ketone salt supplement 2. Fasting with exogenous carbohydrate supplement

Interventions

DIETARY_SUPPLEMENTexogenous ketone salt supplement

Dietary Supplement: Fasting water and with exogenous ketone salt supplement. Participants will have to take 1 doses of supplement 30 minutes before the scan.

DIETARY_SUPPLEMENTexogenous carbohydrate supplement

Dietary Supplement: Fasting water and with exogenous carbohydrate supplement. Participants will have to take 1 doses of supplement 30 minutes before the scan.

Sponsors

Nestlé Health Science
CollaboratorINDUSTRY
Université de Sherbrooke
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Masking description

Triple (Participant, Investigator, Outcomes Assessor) Investigators, participants and outcome assessors will be fully blinded.

Intervention model description

Crossover Assignment, Each participant will have to do the 2 Acute supplementation interventions

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients with heart failure with left ventricle ejection fraction of 40% * Heart failure of ischemic or dilated etiology * Ambulatory patient with a NYHA functional class of II-III; * Stable symptoms and no change in medical therapy in the last month.

Exclusion criteria

* Diabetes * Patients treated with any SGLT2i; * Chronic kidney disease * Acute coronary syndrome in the last 3 months; * Use of parenteral inotropic agents; * Persistent or permanent atrial fibrillation or atrial flutter; * Presence of pacemaker or defibrillator; * Medical condition that causes malabsorption of the test material; * Under ketogenic diet, or using exogenous ketone supplements * Use of nicotinamide adenine dinucleotide (NAD) precursor supplements

Design outcomes

Primary

MeasureTime frameDescription
Left ventricle ejection fraction by cardiac MRI under acute intake of exogenous ketone salt compared with exogenous carbohydrate placebo in heart failure patients.15 minutesMeasure by Cardiac MR in pourcentage between diastolic and systolic volume in millimeter

Secondary

MeasureTime frameDescription
Ventricle volume by cardiac MRI after intake supplement in heart failure patients.15 minutesMeasure by Cardiac MR in millimeter
Cardiac output by cardiac MRI after intake supplement in heart failure patients.15 minutesMeasure by Cardiac MR in liter per minute
Right ventricle ejection fraction by cardiac MRI after intake supplement in heart failure patients.15 minutesMeasure by Cardiac MR in pourcentage between diastolic and systolic volume in millimeter
Effects of supplement on the blood pressure of heart failure patients60 minutesMeasure the blood pressure in systole and diastole in mm Hg
Effects of supplement on the heart rate of heart failure patients60 minutesMeasure the heart rate in beat per minute
Effects of supplement on serum biomarkers60 minutesConcentration of lactate (mmol/L)

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026