Skip to main content
OpenTrials
Enrolling by Invitation

NCT Number: NCT06937320

Chronic Exogenous Ketosis in HFpEF

The goal of this clinical research study is to test what effects a ketone drink will have in people with heart failure with preserved ejection fraction (HFpEF), including on exercise and heart function. Patients with HFpEF often have difficulty exercising, and our goal is to understand whether a ketone drink changes much patients can exercise. The study has three visits, including a baseline visit to assess for study eligibility, and two visits (one after 8 weeks of a ketone drink or a placebo drink, and another one after 8 weeks of whichever drink the participant did not receive the first time).

Enrolling by Invitation

Interested in participating?

Request Info

Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • 18 years of age or older
  • Stable medical therapy for at least 2 weeks
  • New York Heart Association (NYHA) class symptoms II or III
  • Left ventricular ejection fraction ≥ 50%
  • Evidence for elevated filling pressures as follows (at least one of the following between a-d):

a. Mitral early (E)/mitral septal tissue annular (e') velocity ratio > 8 on echocardiography in addition to one of the following:

i. Enlarged left atrium (LA>4.0 cm width or LA volume index >34 mL/m2)

ii. Chronic loop diuretic use for control of symptoms

iii. Elevated natriuretic peptides within the past year (NT-proBNP>125 pg/ml or BNP>35 pg/ml)

b. Mitral E/e' ratio > 14 at rest or with exercise on echocardiography

c. Elevated invasively-determined filling pressures previously (resting left ventricular end-diastolic pressure >16 mm Hg or pulmonary capillary wedge pressure > 14 mmHg; or PCWP or LVEDP ≥ 25 mmHg with exercise)

d. Prior episode of acute heart failure requiring IV diuretics with evidence of volume overload on exam or radiology, or evidence of elevated natriuretic peptides.

Exclusion criteria

  • Intentional ketogenic (high fat, low carbohydrate) diet in the last week
  • Cirrhosis or alcohol use disorder (>14 drinks/week).
  • Contraindications to stress testing, conditions that limit exercise, and other clinically-significant causes of exertional limitation (claudication with peripheral artery disease, atrial fibrillation and heart rate >110 at rest, systolic blood pressure>180 mmHg or diastolic blood pressure>110 mmHg, infiltrative/hypertrophic/inflammatory cardiomyopathy, clinically significant pericardial disease, joint or neuromuscular disease that precludes exercise, acute coronary syndrome within the last 2 months, estimated glomerular filtration rate<20 mL/min/1.73 m2, and hemoglobin < 9 mg/dL).
  • Clinically significant lung disease, defined as severe obstructive lung disease (Gold stage 3), a requirement for supplemental oxygen, or chronic obstructive pulmonary disease with an exacerbation requiring steroids or antibiotics within the last 2 months.
  • > Moderate aortic stenosis, >mild mitral stenosis, > moderate aortic or mitral regurgitation on screening echocardiogram, or presence of a prosthetic valve in the mitral position.
  • Type 1 diabetes mellitus
  • Start of a GLP-1 RA within the past 6 months.
  • Pregnant women.
  • Angina due to epicardial coronary disease or known presence of clinically-significant, unrevascularized epicardial coronary disease, in the investigator's opinion.
  • Prior reduced LVEF to < 45% by echocardiography or cardiac MRI
  • Participation in another clinical study with an investigational product in the previous 4 weeks prior to enrollment (or longer if deemed necessary by the investigator).
  • Conditions that may render the patient unable to complete the study, in the opinion of the investigator.

Treatment and study plan

Exogenous Ketone Drink

Dietary Supplement

(R)-1,3-butanediol (BD, commercially available as "KetoneIQ") initially dosed 300 mg/kg BID (target dose 400 mg/kg grams BID if tolerated) for 8 weeks

Other names: (R)-1,3-butanediol, KetoneIQ, ketone

Placebo

Dietary Supplement

equi-volume placebo administered for 8 weeks

Primary outcomes

  1. Maximal exercise capacity

    Time frame: 8 weeks

    Peak VO2 assessed by cardiopulmonary exercise testing

Secondary outcomes

  1. Respiratory exchange ratio

    Time frame: 8 weeks

    Respiratory exchange ratio (RER) during cardiopulmonary exercise testing at 25 watts

  2. Vasodilatory reserve

    Time frame: 8 weeks

    Percent change in total peripheral resistance from rest to peak exercise

  3. Left atrial volume index

    Time frame: 8 weeks

    Left atrial volume index measured by echocardiogram

  4. Resting E/e'

    Time frame: 8 weeks

    Resting E/e' on echocardiogram

  5. Heart failure-related health status

    Time frame: 8 weeks

    Heart failure-related health status using Kansas City Cardiomyopathy Questionnaire overall summary score (KCCQ-OSS). Score range is from 0 to 100, with higher scores indicating better health status and lower scores indicating poorer health status.

  6. NT-proBNP

    Time frame: 8 weeks

    N-terminal pro-B-type natriuretic peptide levels measured in peripheral blood.

Other outcomes

  1. Global longitudinal strain

    Time frame: 8 weeks

    Global longitudinal strain measured by echocardiogram

  2. Exercise E/e' ratio

    Time frame: 8 weeks

    Measured during exercise as the ratio of early diastolic transmitral flow velocity (E) to early diastolic mitral annular velocity (e')

  3. Hemoglobin A1c

    Time frame: 8 weeks

    Hemoglobin A1c level measured in peripheral blood

  4. Fat free mass

    Time frame: 8 weeks

    Fat free mass measured by body composition scan (DXA)

  5. Pulse wave velocity

    Time frame: 8 weeks

    Pulse wave velocity measured during arterial tonometry

  6. Ventilatory efficiency

    Time frame: 8 weeks

    VE/VCO2 slope during cardiopulmonary exercise testing

Sponsors and collaborators

Lead sponsor

Duke University

Other

Registry information

Official study title

Chronic Effects of Exogenous Ketone Administration in Heart Failure With Preserved Ejection Fraction

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Apr 22, 2025
Registry last updated
Sep 17, 2025

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.

Published trials that share one or more normalized conditions with this study.