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

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McMaster University

Status

Enrolling

Conditions

High Altitude Hypoxia
Exercise

Treatments

Dietary Supplement: Ketone Monoester (KME)
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT07063732
KETEX_WM

Details and patient eligibility

About

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.

Enrollment

14 estimated patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

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

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

14 participants in 2 patient groups

High Altitude (3800m; Barcroft Research Station)
Experimental group
Description:
High altitude setting
Treatment:
Dietary Supplement: Placebo
Dietary Supplement: Ketone Monoester (KME)
Low Altitude (334m; University of Guelph)
Experimental group
Description:
Low altitude setting
Treatment:
Dietary Supplement: Placebo
Dietary Supplement: Ketone Monoester (KME)

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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