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Clinical Trials in Canada / NCT07063732
Recruiting Not applicable

Ketone Monoester Supplements, High Altitude, and Brain Blood Flow During Exercise

NCT07063732 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2025-05-28
Last updated
2025-07-14

Condition(s) studied

High Altitude HypoxiaExercise

Investigational drug(s) / intervention(s)

Ketone Monoester (KME)Placebo

Ketone Monoester (KME): 0.6 g KME per kg body mass; \[R\]-3-hydroxybutyl \[R\]-3-hydroxybutyrate. (Delta G Ketone, TΔS, Oxford).

Placebo: Inert, calorie-free placebo drink that is taste-matched to the ketone monoester supplement

Study summary

The purpose of this trial is to investigate the effect of acute ketone monoester ingestion (0.6 g KME/kg body weight) on the occurrence of the ventilatory threshold and the subsequent response of blood velocity in cerebral arteries during a maximal exercise test at low altitude and high altitude.

Eligibility

Sex
ALL
Min age
18 Years
Max age
35 Years
Healthy volunteers
Accepted
Inclusion Criteria: \- Must be a member of the research expedition team travelling to the Barcroft Research Station in White Mountain California Exclusion Criteria: * BMI \> 30 * No prescribed medications (oral contraceptives excluded) * History of smoking * Currently following a ketogenic diet or consuming exogenous ketogenic supplements * History of heart, lung, blood vessel, or kidney disease * Currently pregnant

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Barcroft Research Station Bishop California Recruiting
University of Guelph Guelph Ontario Recruiting

More McMaster University trials in Canada

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 NCT07063732 on ClinicalTrials.gov ↗ ← All trials in Canada