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Completed

NCT Number: NCT05768100

Hemodynamic Effects of Modulating Circulating Ketone Bodies With 1,3-butanediol

Heart Failure (HF) is a major public health issue affecting 1-2% of the Western population and the lifetime risk of HF is 20%. Despite major improvements in the management and care of patients with HF, the 1-year mortality in patients with HF is high. Furthermore, patients with HF have markedly decreased physical capacity and quality of life. Thus, there is a need for new treatment modalities in this group of patients.

In a first-in-man study we have recently discovered that 3-OHB-infusion increases cardiac output by 2 L/min (40% relative increase) and left ventricular (LV) ejection fraction (LVEF) by 8% in absolute numbers in patients with HF and reduced LVEF (HFrEF).

1,3-Butanediol (BD) serves as a potential nutritional supplement in providing long-lasting ketosis as a treatment option in heart disease. Whether BD provides similar hemodynamic effects as ketone monoester remains unknown.

Hypothesis Oral BD increases cardiac output and LV function in patients with HFrEF.

Aims To investigate the acute hemodynamic effects of weight-adjusted oral BD supplements in patients with HFrEF.

Design In a randomized, single-blind, placebo-controlled, crossover design, 12 patients with HFrEF are studied following overnight fast on 2 separate visits in random order: 1) during intake of BD (HVMN, San Francisco, California, USA) and during placebo.

Methods Transthoracic echocardiography, non-invasive blood pressure, and venous blood samples are obtained every 60 minutes from baseline until 6 hours following BD ingestion.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Dept. of Cardiology, Aarhus University Hospital

Aarhus, Denmark

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Chronic HF: NYHA class II-III, LVEF <40%. Negative urine-HCG for women with childbearing potential. Age ≥18 years.

Exclusion criteria

  • Diabetes or HbA1c >48 mmol/mol, significant cardiac valve disease, severe stable angina pectoris, severe comorbidity as judged by the investigator, inability to give informed consent.

Treatment and study plan

1,3-Butanediol

Dietary Supplement

1,3-Butanediol

Other names: Ketone-IQ (HVMN)

Placebo

Dietary Supplement

Isovolumic placebo

Primary outcomes

  1. Cardiac output

    Time frame: 6 hours

    As measured by LVOT VTI and HR

Secondary outcomes

  1. Stroke volume

    Time frame: 6 hours

  2. Heart rate

    Time frame: 6 hours

  3. LVEF

    Time frame: 6 hours

  4. Changes in circulating 3-OHB

    Time frame: 6 hours

  5. Changes in FFA

    Time frame: 6 hours

Sponsors and collaborators

Lead sponsor

Aarhus University Hospital

Other

Registry information

Acronym: KETO-BD

Important dates

Study start
2023
Primary completion
2023
Study completion
2024
First posted
Mar 14, 2023
Registry last updated
Mar 22, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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