← Back to Clinical Trials
Recruiting NCT05594706

NCT05594706 Anhydroglucitol in Children With Type 1 Diabetes

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT05594706
Status Recruiting
Phase
Sponsor University Hospital, Geneva
Condition Diabetes Mellitus, Type 1
Study Type OBSERVATIONAL
Enrollment 60 participants
Start Date 2023-01-27
Primary Completion 2026-12-31

Eligibility & Interventions

Sex All sexes
Min Age 2 Years
Max Age 18 Years
Study Type OBSERVATIONAL
Interventions
Measurement of blood levels of 1,5-anhydroglucitol

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 60 participants in total. It began in 2023-01-27 with a primary completion date of 2026-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The investigators will measure blood levels of 1,5-anhydroglucitol in children with type 1 diabetes and correlate them with parameters related to functional beta-cell mass in diabetic patients. The values will be compared to those obtained in healthy volunteers. Children with newly diagnosed diabetes as well as children with longstanding disease will be included. The aim of the study is to test the validity of 1,5-anhydroglucitol as a novel biomarker of beta-cell mass and function in type 1 diabetes.

Eligibility Criteria

Inclusion Criteria: * Type 1 diabetes with positive autoantibodies against islets, insulin, islet antigen 2 (IA2), glutamic acid decarboxylase (GAD) 65 or zinc transporter (ZnT)8. * Treatment with continuous subcutaneous insulin infusion (CSII) with or without automated insulin delivery (AID). * Monitoring with a continuous glucose measurement system (CGMS) or flash glucose monitor (FGM). * Patient willing to keep the same type of CGMS or FGM during the year of observation * Ability to give informed consent as documented by signature Exclusion Criteria: * Patients treated with multiple daily injections (MDI) or not willing to wear a CGMS of FGM * Patients changing the type of CGMS during the course of the study.

Contact & Investigator

Central Contact

Philippe Klee

✉ philippe.klee@unige.ch

📞 +41 22 372 45 90

Frequently Asked Questions

Who can join the NCT05594706 clinical trial?

This trial is open to participants of all sexes, aged 2 Years or older, up to 18 Years, studying Diabetes Mellitus, Type 1. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05594706 currently recruiting?

Yes, NCT05594706 is actively recruiting participants. Contact the research team at philippe.klee@unige.ch for enrollment information.

Where is the NCT05594706 trial being conducted?

This trial is being conducted at Geneva, Switzerland.

Who is sponsoring the NCT05594706 clinical trial?

NCT05594706 is sponsored by University Hospital, Geneva. The trial plans to enroll 60 participants.

Related Trials

Related Intelligence Guides

In-depth guides covering this condition's trials, eligibility, and what to expect.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology