Ireland
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Recruiting Observational

French National Cohort of People With Type 1 Diabetes

NCT04657783 · tracked via the Priya Life Science France tracker
Sponsor
Fondation Francophone pour la Recherche sur le Diabete
Phase
Observational
Started
2020-06-10
Last updated
2023-02-15

Condition(s) studied

Diabetes Mellitus, Type 1Cardiovascular DiseasesHypoglycemiaPatient Participation

Study summary

Cardiovascular (CV) diseases are the most frequent type 1 diabetes (T1D) complications. A recent epidemiological study showed that patients with T1D have a two-fold CV mortality risk, even in case of good glycemic control. In addition, it has been shown that patients with T1D with no traditional CV risk factors had about a 80% higher risk of cardiovascular event compared to non-diabetic individuals. This indicates that further modifiable risk factors in relation to CV mortality remain to be identified.

One of the candidates that could help to disentangle the factors associated with the increased CV mortality in T1D patients is glycemic variability which could contribute to diabetes complications. Indeed, severe hypoglycaemia, one of the most severe consequence of glycaemic variability, are associated with a higher mortality in patients with type 1 and type 2 diabetes.

In order to evaluate the relation between glycemic variability, insulin therapy modalities and CV risk as well as some other questions related to health determinants of T1D, we are building up a large observational, prospective, multi-centric cohort study of patients gathering 15,000 patients with T1D, age above 6 years old, to perform the following:

* Collecting clinical information
* Evaluating Glycemic variability (assessed by the coefficient of variation of glucose (CV) calculated from automatically downloaded continuous glucose monitoring data (CGM)
* Biobanking including plasma, DNA, urine, saliva and hair.
* Collecting patients' reported outcomes through auto-questionnaires (online questionnaires).
* Doing an active follow-up for a period of 10 years with an intermediate visit every 3 years.
* Passive follow-up: link to national Health data system (Système National de Données de Santé, SNDS) in order to exhaustively collect health events as death, CV events and hospitalizations (including severe hypoglycemia).

Eligibility

Sex
ALL
Min age
6 Years
Max age
100 Years
Healthy volunteers
No
1. Inclusion Criteria * Adults and children (age \>= 6 years) * Type 1 diabetes, defined as: * Age at diagnosis of diabetes \> 1 year and \<= 35 years * Insulin treatment initiated within the first 12 months following diabetes discovery * Affiliation to the French social security scheme (RIPH-2 constraint) * Ability to speak and read French * Ability to give written informed consent 2. Non-inclusion Criteria Patient under guardianship or protection for vulnerable people

Primary outcome measure(s)

  • Major adverse cardiovascular events (MACE) — 30 years
    The MACE will include non-fatal myocardial infarction (MI), non-fatal stroke, and CV-related death (defined as a death occurring within 30 days after a diagnosis for MI, stroke, unstable angina, heart failure, sudden cardiac arrest, cardiogenic shock, other cerebrovascular events, or other CV events recorded in a medical claim in any setting).

Trial sites (1)

FacilityCityRegionStatus
FFRD Paris France Recruiting
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 NCT04657783 on ClinicalTrials.gov ↗ ← All trials in France