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Clinical Trials in Czechia / NCT07527156
Recruiting Phase 4

Prolonged Nasogastric Administration of Ketones in Decompensated Heart Failure

NCT07527156 · tracked via the Priya Life Science Czechia tracker
Phase
Phase 4
Started
2026-04-04
Last updated
2026-04-14

Condition(s) studied

Acute Heart Failure (AHF)Cardiogenic ShockHeart FailureKetonesKetone Body Metabolism

Investigational drug(s) / intervention(s)

Ketone Monoester (KE)

Ketone Monoester (KE): Continous infusion of a commercially available ketone monoester via nasogastric tube.

Study summary

This study will evaluate the feasibility and safety of achieving therapeutic concentrations of beta-hydroxybutyrate using continuous infusion of D-beta-hydroxybutyrate monoester administered via a nasogastric tube in patients with acutely decompensated heart failure with reduced left ventricular ejection fraction.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * LVEF \<35% * Acute heart failure with low cardiac output syndrome or cardiogenic shock Exclusion Criteria: * Severe liver failure * Severe acidosis * Inability to insert nasogastric tube * Gastric paralysis / ileus * Repeated vomiting * Severe hypokalemia

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Institute for Clinical and Experimental Medicine (IKEM) Prague Prague Recruiting

More Institute for Clinical and Experimental Medicine trials in Czechia

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07527156 on ClinicalTrials.gov ↗ ← All trials in Czechia