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Clinical Trials in Denmark / NCT07774780
Starting soon Not applicable

Oral Galactose as a Substrate for Post-Exercise Skeletal Muscle Glycogen Repletion in Individuals With Type 1 Diabetes

NCT07774780 · tracked via the Priya Life Science Denmark tracker
Phase
Not applicable
Started
2027-02-01
Last updated
2026-08-19

Condition(s) studied

Type 1 Diabetes

Investigational drug(s) / intervention(s)

galactose

galactose: Participants undergo two experimental conditions in a randomized crossover design. In one condition, participants ingest 30 g of galactose, whereas in the other condition, they ingest 30 g of galactose combined with 30 g of glucose. The order of the conditions is randomized across participants.

Study summary

This Ph.D. project investigates whether orally ingested galactose can be taken up by skeletal muscle and the heart in response to exercise or hyperinsulinemia, and whether it may serve as a viable nutritional strategy for individuals with type 1 diabetes (T1D).

Although exercise provides significant health benefits for people with T1D, it is often associated with substantial glucose fluctuations and an increased risk of hypoglycemia. Conventional carbohydrate strategies based on glucose may further exacerbate glycemic instability due to the rapid increase in blood glucose levels. In contrast, galactose is metabolized more slowly and may therefore provide a more stable energy source during and after exercise.

Previous research has demonstrated that intravenously administered galactose is taken up by human skeletal muscle, with uptake increasing during exercise, suggesting a mechanism that may be at least partly insulin-independent. Building on these findings, this project aims to determine whether similar uptake occurs when galactose is ingested orally.

This study uses a randomized controlled design and applies non-invasive 18F-FDGal PET imaging to quantify galactose uptake in skeletal muscle and cardiac tissue. The findings may contribute to improving dietary recommendations for individuals with T1D, particularly in relation to maintaining stable blood glucose levels during and after physical activity.

Eligibility

Sex
ALL
Min age
20 Years
Max age
70 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Healthy or T1D * BMI 18,5-30 kg/m2 * Singed informed consent Exclusion Criteria: * Clinically significant heart, lung, kidney, liver, endocrine, or malignant disease based on information collected during the initial screening visit as well as blood tests * Lack of awareness of hypoglycemia episodes * Blood donation within the last 3 months * Smoking * Alcohol or substance abuse * Participation in other studies involving ionizing radiation within the last 6 months * Claustrophobia * Inability to train one leg for one hour

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Aarhus Universitet Aarhus Denmark
steno diabetes center Aarhus Aarhus Denmark

More University of Aarhus trials in Denmark

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07774780 on ClinicalTrials.gov ↗ ← All trials in Denmark