Monitoring Blood Sugar Swings to Predict Early Type 1 Diabetes
Tests glucose monitors in people with early type 1 diabetes signs.
Plain-language title generated from the registry record
Registry title: Continuous Monitoring of Glycemic Variability to Predict Dys- and Hyperglycemia in Asymptomatic Type 1 Diabetes
Key facts
- Where
- Antwerp, Bruges, Ghent, Jette, Leuven, and Liège, BelgiumSee the 6 sites
Could this be for you?
Answer for yourself. This is not a decision: only the study team can say whether you can take part.
- Are you between 5 and 39 years old?
Source: NCT05777330, who can take part
Where in Belgium
- Universitair Ziekenhuis AntwerpenAntwerp, BelgiumTaking people
- A.Z. Sint-Jan BruggeBruges, BelgiumTaking people
- Universitair Ziekenhuis GentGhent, BelgiumTaking people
- Universitair Ziekenhuis BrusselJette, BelgiumTaking people
- Universitair Ziekenhuis LeuvenLeuven, BelgiumTaking people
- Clinique CHC MontLégiaLiège, BelgiumTaking people
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Universitair Ziekenhuis Brussel
- Trial code
- NCT05777330
- Record updated
- 17 August 2026
- Original description
The goal of this longitudinal clinical trial is to measure variability of interstitial glucose levels with a user-friendly real-time continuous glucose monitoring (CGM) technology at regular intervals in normo- and dysglycemic multiple autoantibody-positive individuals (age 5-39 years), in comparison with single autoantibody-positive individuals in the same age range. Participants will asked to undergo repeated oral glucose tolerance tests (OGTTs) (age 5-39 years) and hyperglycemic clamp tests (age 12-39 years) in parallel for a period of at least 2-3 years. In case of confirmed dysglycemia, we propose to perform CGM and OGTT every 3 months.Read full original descriptionShow less
Continuous Monitoring of Glycemic Variability to Predict Dys- and Hyperglycemia in Asymptomatic Type 1 Diabetes
The goal of this longitudinal clinical trial is to measure variability of interstitial glucose levels with a user-friendly real-time continuous glucose monitoring (CGM) technology at regular intervals in normo- and dysglycemic multiple autoantibody-positive individuals (age 5-39 years), in comparison with single autoantibody-positive individuals in the same age range. Participants will asked to undergo repeated oral glucose tolerance tests (OGTTs) (age 5-39 years) and hyperglycemic clamp tests (age 12-39 years) in parallel for a period of at least 2-3 years. In case of confirmed dysglycemia, we propose to perform CGM and OGTT every 3 months.
The main questions the study aims to answer are:
1. Do the amplitude and time trends of CGM-derived glycemic variability indices and OGTT- and clamp-derived variables differ between the intermediate, high and very high risk groups? 2. Can (changes in) CGM-derived glycemic variability indices predict/detect dysglycemia in initially normoglycemic (single or multiple autoantibody-positive) individuals with the same diagnostic efficiency as OGTT- or clamp-derived variables? 3. Can (changes in) CGM-derived glycemic variability indices predict clinical onset in (stage 1 or 2) multiple autoantibody-positive individuals with the same diagnostic efficiency as OGTT- or clamp-derived variables? 4. Can correlating (changes in) CGM-derived indices with (changes in) OGTT- and clamp-derived variables help to better understand the sequence of events leading to dysglycemia and clinical onset, as well as the relative contribution of beta cell function and insulin action to glycemic variability according to disease stage and biological and phenotypical characteristics of the individuals?
Inclusion: aged 5-39 years at inclusion; absence of diabetes meeting the clinical diagnostic American Diabetes Association (ADA) criteria; persistently positive for one or multiple types of autoantibodies among IAA, GADA, IA-2A and ZnT8A.
Exclusion: Treatment with immune modulating or diabetogenic medication (e.g. corticosteroids) or medication that act to lower glycemia (oral antidiabetics) or agents that may influence insulin sensitivity or secretion; Diabetes meeting the clinical diagnostic ADA criteria; Use of illicit drugs, or overconsumption of alcohol, or history of drug or alcohol abuse; Being legally incapacitated, having significant emotional problems at the time of the study, or having a history of psychiatric disorders; History of acute or chronic pancreatitis, or (partial) pancreatectomy; History of any illness that, in the opinion of the investigator, might confound the results of the study or pose additional risks to the subjects; Pregnancy or lactation in women; <6 months postpartum; Gastric bypass or banding.