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NCT05917873Completed

Metabolic Effects of Four-week Lactate-ketone Ester Supplementation

Source: ClinicalTrials.gov · Last updated 28 Aug 2025

Brief summary (registry, in English)

Recent research reveals intriguing results concerning the role of exogenous lactate and the ketone body 3-hydroxybutyrate (3-OHB) as therapeutic tools to combat obesity and related conditions. Thus, oral administration of lactate and 3-OHB have separately been shown to suppress appetite sensations and slow gastric emptying while administered orally. Both seem to inhibit lipolysis while oral 3-OHB administration have shown direct insulin sensitizing effects. Furthermore, both substrates can be used as fuel for the heart. The goal of this placebo-controlled randomized crossover design is to test exogenous lactate and the ketone body 3-hydroxybutyrate (3-OHB) in healthy, non-diabetic, obese adults. The main questions it aims to answer are if chronic administration of LaKe ester affect or improve the following endpoints: * Insulin sensitivity * Appetite sensations * Gastric emptying * Lipolysis * Cardiac output * Left Ventricular Ejection Fraction * Global Longitudinal Strain and other echocardiographic measures listed below Participants will ingest a combined lactate and ketone body ester (LaKe ester) or placebo twice a day for 28 days before experimental days.

Status (registry)
Completed
Study type
Interventional
Enrollment
10 (actual)
First submitted
5 Jun 2023
Start date
7 Sept 2023
Primary completion date
11 Dec 2024
Lead sponsor
University of Aarhus
Diseases
Obesity
NCT number
NCT05917873

What you commit to

  • Study type: Interventional
  • Participants enrolled: 10
  • From 7 Sept 2023 to the primary completion date, 11 Dec 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Cardiac arrhythmias (eg atrial fibrillation)
  • Ongoing acute/chronic serious diseases (eg, anemia, chronic kidney or liver disease)

Lab values

  • Medication that affect energy or glucose metabolism, eg metformin, insulin or Glucagon-like peptide-1 receptor (GLP-1) agonists

Other

  • Specific diets (eg practicing ketogenic diets)
  • Inability to understand Danish or English

Who the study is looking for

  • Age between 30-60 years
  • BMI range 30-40
  • Glycated haemoglobin (HbA1c) \< 48 mmol/mol
  • Otherwise 'healthy'
  • Written and oral consent

Age in the registry: 30 years to 60 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
steno diabetes center Aarhus
Coordinator of this site? Confirm its status
AarhusDenmarkUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.