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The Effect of Acute Exogenous Oral Ketone Supplementation on Immune Cells Function and Immune Cells Histone Β-hydroxybutyrylation (Acute_Ketone)

University of British Columbia logo

University of British Columbia

Status

Enrolling

Conditions

Histone Deacetylase (HDAC) Activity
Immune Functions
Ketosis, Metabolic

Treatments

Dietary Supplement: Ketone Monoester (KE)

Study type

Interventional

Funder types

Other

Identifiers

NCT06590623
H24-02548

Details and patient eligibility

About

To conduct a single-arm pilot study to determine how acute ingestion of an exogenous ketone monoester supplement alters the histone lysine β-hydroxybutyrylation and immune function in healthy human monocytes and lymphocytes.

Enrollment

12 estimated patients

Sex

All

Ages

19+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Over the age of 19
  • Able to fast overnight

Exclusion criteria

  • Being a competitive endurance athlete.
  • Following a ketogenic diet, low-calorie diet, periodic fasting regimen, or regularly consuming ketogenic supplements.
  • Being unable to travel to and from the university
  • Being pregnant.
  • Having been diagnosed with a chronic disorder of glucose or fat metabolism, including type 2 diabetes, chronic pancreatitis, or gallbladder disease
  • Being unable to read or communicate in English.

Trial design

Primary purpose

Basic Science

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

12 participants in 1 patient group

exogenous ketone supplement
Experimental group
Description:
Participants will consume a ketone monoester supplement (KetoneAid KE4) at a dose of 0.75 g/kg of body weight.
Treatment:
Dietary Supplement: Ketone Monoester (KE)

Trial contacts and locations

1

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Central trial contact

Jonathan Little Principal Investigator, Professor Little, Ph.D

Data sourced from clinicaltrials.gov

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