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CompletedNCT03073356Updated Dec 11, 2017

Ketones in Heart Failure - Effects on Cardiac Efficiency

A Phase 2 interventional study of Infusion of 3-OHB and Infusion of placebo in Heart Failure, Systolic and Ketonemia, sponsored by University of Aarhus. Completed at 1 site in Denmark. Open to participants aged 18 Years to 90 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-12-11.

Sponsored by University of Aarhus · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
44
Allocation
Randomized
Ages
18 Years to 90 Years
Sex
All
01

Study summary

Ketones may have beneficial effects on myocardial metabolism and hemodynamics. In the present study, healthy test subjects and patients with heart failure with reduced ejections fraction will be investigated in a randomized cross-over design with ketone infusions and placebo. Myocardial efficiency and hemodynamics will be evaluated.

Read the detailed description

The prevalence of patients with heart failure and reduced ejection fraction (HFrEF) is 1-2%, and the lifetime risk of heart failure at age 55 years is approximately 30%. Despite advances in treatment, hospitalization rate and mortality remains high. It is well known that myocardial metabolism changes during development of HFrEF, and may contribute to contractile dysfunction. However, the myocardium can be considered an omnivore regarding substrate utilization, conferring an important adaptive property. Hence, it metabolizes either glucose, lipids, lactate, amino acids or ketones (3-hydroxybutyrate) depending on substrate availability, hormonal status and cardiac demands. These substrates differ with regard to myocardial energy efficiency (MEE) (cardiac work related to oxygen consumption). Since high MEE is associated with a better prognosis in HFrEF, manipulating substrate uptake could be a new treatment modality in heart failure patients.

Recently, it was shown that the human myocardium increases 3-hydroxybutyrate (3-OHB) metabolism during development of HFrEF. These changes may be beneficial as 3-OHB could increase myocardial efficiency and lower oxidative stress by scavenging free radicals. However, until now this has not been investigated in clinical trials, and the effect of 3-OHB on cardiac function, oxygen consumption and perfusion remains undetermined in HFrEF patients.

In the present study the investigators will evaluate whether elevated circulating 3-OHB affect myocardial oxygen consumption, MEE and perfusion in healthy subjects and patients with HFrEF, and whether 3-OHB affect hemodynamics and contractile function.

10 healthy test subjects and 20 HFrEF patients will be subjected to placebo and 3-OHB infusion in a randomized cross-over design. Acetate-PET, echocardiography and right sided heart catheterization will be applied.

02

Conditions studied

  • Heart Failure, Systolic
  • Ketonemia

Keywords

  • Myocardial metabolism
  • Positron emission tomography
  • Echocardiography
  • Right sided heart catheterization
03

In context

Heart Failure

5,701 studies on the registry are indexed under Heart Failure; 1,220 are open to participants now.

This study's enrollment of 44 is below the median of 72 across 3,736 interventional studies indexed under Heart Failure.

Browse Heart Failure studies →

Lead sponsor

University of Aarhus is the lead sponsor of 1,274 studies on the registry; 183 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • For participants with heart failure:
  • Symptoms of Heart failure NYHA 2-3
  • LVEF\<40%

For all participants:

  • Negative HCG for women in the pregnant age

Exclusion criteria

Exclusion Criteria:

  • Significant cardiac valve disease
  • Signs or history of major myocardial infarction (STEMI) within 3 months
  • Other disease or treatment making subject unsuitable for study participation
  • Treatment for diabetes or HbA1c level >7%
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Masking
Triple (Participant, Investigator, Outcomes assessor)
Enrollment
44 participants (actual)

Study arms

  • Experimental
    Control - Healthy test subjects

    Age matched subjects without symptoms of heart failure or ischemic heart disease N=10

    Biological: Infusion of 3-OHB · Biological: Infusion of placebo

  • Experimental
    HFrEF - Heart failure patients investigated by PET

    Patients with heart failure (HFrEF) N=12

    Biological: Infusion of 3-OHB · Biological: Infusion of placebo

  • Experimental
    HFrEF - Right heart catheterization

    Patients with heart failure (HFrEF) N=12

    Biological: Infusion of 3-OHB · Biological: Infusion of placebo

  • Experimental
    HFrEF - Right heart catheterization study 2

    Dose finding study (increasing dosage of 3-OHB)

    Biological: Infusion of 3-OHB · Biological: Infusion of placebo

Interventions

  • BiologicalInfusion of 3-OHB

    Increase in 3-OHB levels

    Also known as: Na-3-OHB

  • BiologicalInfusion of placebo

    NaCl

    Also known as: NaCl

06

What researchers measure

Primary outcomes

  1. Myocardial efficiency

    Based on myocardial PET examinations

    Time frame: 1 day

  2. Cardiac output

    Right sided heart catheterization

    Time frame: 1 day

Secondary outcomes

  1. Myocardial perfusion

    Based on myocardial PET examinations

    Time frame: 1 day

  2. Myocardial oxygen consumption

    Based on myocardial PET examinations

    Time frame: 1 day

  3. Pulmonary and wedge pressure

    Right sided heart catheterization

    Time frame: 1 day

  4. Mixed venous saturation

    Right sided heart catheterization

    Time frame: 1 day

07

Study locations

1 site
  • Dept. of cardiology, Aarhus university hospital Skejby
    Aarhus, Region Midtjylland 8200, Denmark
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 11, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03073356
Lead sponsor
University of Aarhus
Responsible party
Sponsor
First posted
Mar 8, 2017
Start date
Mar 17, 2017
Primary completion
Nov 16, 2017
Completion
Nov 16, 2017
Last update
Dec 11, 2017

Study contacts

Roni R Nielsen, MD PHD
principal investigator · Dept. of Cardiology

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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