Duke University
Durham, North Carolina, 27710, United States
NCT Number: NCT06937320
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).
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
Durham, North Carolina, 27710, United States
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
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
(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
equi-volume placebo administered for 8 weeks
Time frame: 8 weeks
Peak VO2 assessed by cardiopulmonary exercise testing
Time frame: 8 weeks
Respiratory exchange ratio (RER) during cardiopulmonary exercise testing at 25 watts
Time frame: 8 weeks
Percent change in total peripheral resistance from rest to peak exercise
Time frame: 8 weeks
Left atrial volume index measured by echocardiogram
Time frame: 8 weeks
Resting E/e' on echocardiogram
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.
Time frame: 8 weeks
N-terminal pro-B-type natriuretic peptide levels measured in peripheral blood.
Time frame: 8 weeks
Global longitudinal strain measured by echocardiogram
Time frame: 8 weeks
Measured during exercise as the ratio of early diastolic transmitral flow velocity (E) to early diastolic mitral annular velocity (e')
Time frame: 8 weeks
Hemoglobin A1c level measured in peripheral blood
Time frame: 8 weeks
Fat free mass measured by body composition scan (DXA)
Time frame: 8 weeks
Pulse wave velocity measured during arterial tonometry
Time frame: 8 weeks
VE/VCO2 slope during cardiopulmonary exercise testing
Duke University
Other
Chronic Effects of Exogenous Ketone Administration in Heart Failure With Preserved Ejection Fraction
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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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