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ENROLLING BY INVITATION
NCT07166965
NA

Ketone and Hawthorn Extract Supplementation in Congestive Heart Failure

Sponsor: Thomas Jefferson University

View on ClinicalTrials.gov

Summary

The purpose of this research is to gain a better understanding of whether supplements can improve heart health. There are a number of study procedures and tests that will occur as a part of the research study. There are 3 groups or arms in the study: one group will receive a ketone supplement, one group will receive hawthorn and a third group will receive a placebo that does not contain ketones or hawthorn. The purpose of the study is to learn whether these supplements improve heart heath in patients who have congestive heart failure. Participants will not know which supplement is received. The study doctor will know. This is called a single blind study. The supplements will provided along with instructions and educational materials. The duration of taking the supplements is approximately 8 weeks and full participation in the study is approximately 3 months. Participants with congestive heart failure will be enrolled through Jefferson Health in Philadelphia, Pennsylvania.

Official title: A Pilot Study of Ketone and Hawthorn Extract Supplementation: Impact on Exercise Capacity, and Heart Function in Patients With Congestive Heart Failure

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

45

Start Date

2025-11-15

Completion Date

2029-09

Last Updated

2025-11-18

Healthy Volunteers

No

Interventions

DIETARY_SUPPLEMENT

Hawthorn supplement

Hawthorn oral supplement

DIETARY_SUPPLEMENT

Ketones

ketone oral supplement

OTHER

Placebo Control

Placebo Control, oral supplement

Locations (1)

Thomas Jefferson University

Philadelphia, Pennsylvania, United States