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N/A N=10 Basic Science

Effect of MCT Emulsification on Ketogenesis in Human Adults

Healthy

Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Dec 2018
Primary outcome: Primary: Plasma Ketone Concentration — 136.97; 177.43; 270.61; 249.3 µmol/L

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
MCT oil 10g (Dietary_supplement); MCT homogenate 10g (Dietary_supplement); Control (Dietary_supplement); MCT oil 20g (Dietary_supplement); MCT homogenate 20g (Dietary_supplement); MCT oil 30g (Dietary_supplement); MCT homogenate 30g (Dietary_supplement)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Université de Sherbrooke
Primary completion
Sep 2014

Outcome Measures

OutcomeResultp-value
PRIMARY
Plasma Ketone Concentration
136.97; 177.43; 270.61; 249.3; 262.92; 277.25
SECONDARY
Plasma Glucose Concentration
4.86; 4.98; 4.97; 4.99; 5.01; 4.84
SECONDARY
Plasma Free Fatty Acids Concentration
0.43; 0.39; 0.41; 0.38; 0.44; 0.41
SECONDARY
Plasma Insuline Concentration
9.79; 13.7; 10.88; 13.00; 12.87; 11.94
SECONDARY
Number of Participants With Side Effects for Each Visit
0; 1; 4; 5; 2; 4

Summary

Lower brain glucose uptake is present before the onset of cognitive deterioration and may increase the risk of cognitive decline in Alzheimer's disease. Ketones are the brain's main alternative energy substrates. Medium-chain triglycerides (MCT) are rapidly beta-oxidized and are ketogenic. Large doses of MCT oil are linked to gastro-intestinal side effects due to incomplete absorption so the investigators examined whether homogenisation into a skim milk matrix (MCT-H) would both improve ketogenesis and reduce side-effects compared to MCT taken without homogenisation into a matrix (bulk MCT [MCT-B]). Hypotheses: (i) MCT-H will be better absorbed compared to MCT-B, so MCT-H will result in higher ketonemia and lower side effects in healthy adults. (ii) The effects of MCT-B and MCT-H on ketogenesis will be dose-dependent.

Eligibility Criteria

Inclusion Criteria

  • aged 18 years or more

Exclusion Criteria

  • smoker
  • pregnancy or breastfeeding
  • diabetes or insulin resistance
  • uncontrolled thyroid disease, hepatic or renal disease
  • uncontrolled high blood pressure
  • medical treatment influencing lipid or glucide metabolism
  • ongoing or past severe drug or alcohol abuse
  • dementia or psychiatric difficulties or depression
  • chronic immune condition or inflammation
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02409927). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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