Clinical Trials Directory

Trials / Completed

CompletedNCT04194450

Exogenous Ketones in Type 2 Diabetes

The Effect of Acute Exogenous Oral Ketone Supplementation on Blood Glucose Levels in Type 2 Diabetes

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
19 (actual)
Sponsor
University of British Columbia · Academic / Other
Sex
All
Age
20 Years – 69 Years
Healthy volunteers
Not accepted

Summary

Exogenous ketone supplements are proposed to have glucose-lowering potential, provide an alternative fuel for the brain and to enhance cognitive function. No studies have tested whether exogenous ketones can lower blood glucose in people with type 2 diabetes. In addition, the impact of exogenous ketones on brain blood flow, cognitive function or brain-derived neurotrophic factor in humans is unknown. The purpose of this study is to determine if acutely ingesting exogenous ketones, in the form of a ketone monoester drink, can lower glucose and improve measures of brain/cognitive function in humans with type 2 diabetes. Participants will consume a ketone monoester drink or placebo with blood samples, brain blood flow, and cognitive function assessed over 180 minutes. The researchers will also test how the ketone monoester drink impacts appetite and measures of inflammation.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTKetone monoesterAcute ingestion of (R)-3-hydroxybutyl (R)-3-hydroxybutyrate prior to assessment of outcomes.
DIETARY_SUPPLEMENTPlaceboAcute ingestion of taste-matched placebo prior to assessment of outcomes.

Timeline

Start date
2020-01-15
Primary completion
2022-05-20
Completion
2022-05-20
First posted
2019-12-11
Last updated
2025-05-30
Results posted
2023-12-11

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT04194450. Inclusion in this directory is not an endorsement.