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Mechanistic Effect of Ketones on Cerebral Blood Flow (MEKC)

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McMaster University

Status

Completed

Conditions

Cerebrovascular Function
Cerebral Blood Flow

Treatments

Dietary Supplement: Normocapnia
Dietary Supplement: Poikilocapnia

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

Oral supplements containing exogenous ketones have recently become available and represent a novel tool for increasing plasma ketone bodies without the need for dietary restriction. Early evidence suggests that oral ketone supplements may enhance cerebral blood flow (CBF). However, a higher dose of a ketone monoester has been shown to slightly lower blood pH and reduce end-tidal CO2 (PetCO2) due to compensatory hyperventilation, which is accompanied by parallel reductions in CBF. Whether reductions in PetCO2 causes reductions in CBF is currently unknown.

The purpose of this study is to investigate the effect of manipulating PetCO2 at normocapnia (PetCO2 maintained at baseline) or poikilocapnia (no PetCO2 targeting; breathing room air), following the ingestion of a dose of a ketone monoester on CBF and cerebrovascular reactivity to CO2 in young adults.

Enrollment

23 patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Having a normal blood pressure (≤125/≤85 mmHg)
  • Between the ages of 18 and 35

Exclusion criteria

  • Individuals who are obese (body mass index > 30 kg/m^2)
  • Individuals who smoke
  • Individuals with respiratory illnesses
  • A history of type 2 diabetes, hypoglycemia, or cardiovascular diseases (i.e. heart attack, stroke)
  • Individuals currently following a ketogenic diet or taking ketone supplements
  • Individuals with a history of concussion(s) with persistent symptoms
  • Individuals participating in elite-level physical training (i.e. varsity athletics)

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

23 participants in 2 patient groups

Poikilocapnia
Sham Comparator group
Description:
Room air-breathing
Treatment:
Dietary Supplement: Poikilocapnia
Normocapnia
Experimental group
Description:
Breathing air mixture with slightly elevated CO2 to maintain PetCO2 to resting baseline levels
Treatment:
Dietary Supplement: Normocapnia

Trial contacts and locations

1

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Central trial contact

Jeremy J Walsh, PhD

Data sourced from clinicaltrials.gov

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