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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05764850
Other study ID # 2022-02119
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 1, 2023
Est. completion date February 1, 2026

Study information

Verified date February 2023
Source Pediatric Clinical Research Platform
Contact Valerie VS Schwitzgebel, MD
Phone +41 22 372 45 90
Email valerie.schwitzgebel@unige.ch
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this observational study consists of performing cluster analysis to decipher underlying disease mechanisms of type 1 diabetes in children and young adults. To this end, we will combine clinical, laboratory, genetic, transcriptomic, and metabolomic datasets of an extensively phenotyped cohort of children and young adults with type 1 diabetes. We will also assess the risk for cardiovascular diseases in this most vulnerable diabetes cohort.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date February 1, 2026
Est. primary completion date February 1, 2026
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 0 Years to 25 Years
Eligibility Inclusion Criteria (Type 1 Diabetic patients): - Informed consent as documented by signature - Patient's age: between 0 and 25 years old. - Children, adolescents, and young adult patients followed in diabetology. Exclusion Criteria (Type 1 Diabetic patients): - No exclusion criteria Inclusion Criteria (Controls): - Informed consent as documented by signature - Patient's age: 25 less than 6 years of age and 25 between 6 and 25 years old. - Healthy patient Exclusion Criteria (Controls): - Patient receiving treatment affecting metabolic control (ex: systemic corticoids, beta blocker, immunotherapy etc.) - Concomitant disease that may affect the analysis of the results (ex: cancer, active autoimmune disease requiring treatment)

Study Design


Related Conditions & MeSH terms


Intervention

Genetic:
Genome sequencing
100 extensively phenotyped pediatric and young adult patients for genotyping, metabolomic and lipidomic analyses. Polygenic risk scores for type 1 diabetes and cardiovascular disease will be performed. For patients older than 6 years who agree to do a second visit (optional), a Mixed Meal Tolerance Test (MMTT: the gold standard for assessing beta cell function) will be done as well as transcriptomic analysis.

Locations

Country Name City State
Switzerland University Hospital of Geneva Geneva

Sponsors (3)

Lead Sponsor Collaborator
Pediatric Clinical Research Platform University Hospital, Geneva, University of Geneva, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Cluster analysis to decipher underlying mechanisms of type 1 diabetes We will combine clinical, laboratory, genetic, transcriptomic, and metabolomic datasets of an extensively phenotyped cohort of type 1 diabetes patients (Children and young adults).
We will create clinical and genetic correlates with the following clinical parameters: Age at diabetes onset (years), disease duration (years), BMI (kg/m2), diabetes autoantibodies, C-peptide level (pmol/l) and decline over time, HbA1c (%), insulin dose (U/kg/d), ketoacidosis at disease onset (y/n), lipid levels (Total cholesterol, triglycerides, HLD, LDL, Lipoprotein(a)), macro- and microvascular complications, ethnicity, family history for diabetes, associated autoimmune diseases (e.g., autoimmune thyroiditis or celiac disease) and mixed meal tolerance test.
blood sampling and analyses
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