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Recruiting NCT04257877

NCT04257877 Proteomic Analysis in Paediatric Diabetes Type 1 (PAPD)

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Clinical Trial Summary
NCT ID NCT04257877
Status Recruiting
Phase
Sponsor Aristotle University Of Thessaloniki
Condition Diabetes Type 1
Study Type OBSERVATIONAL
Enrollment 50 participants
Start Date 2018-11-20
Primary Completion 2025-01-20

Trial Parameters

Condition Diabetes Type 1
Sponsor Aristotle University Of Thessaloniki
Study Type OBSERVATIONAL
Phase N/A
Enrollment 50
Sex ALL
Min Age 5 Years
Max Age 10 Years
Start Date 2018-11-20
Completion 2025-01-20
Interventions
Blood sampling

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Brief Summary

The aim of the present study is to investigate a targeted proteomic analysis in plasma of children - of Greek origin- with type 1 diabetes (DT1) and its correlation with the electrophysiological findings that accompany diabetic peripheral neuropathy. Diabetic neuropathy is the most frequent chronic complication in adults with DT1 and rarely appears in childhood. Nevertheless, cases of acute mononeuritis have been described at the time of diagnosis of DT1. According to recent reports several biomarkers, including proteomic analysis, have been proposed for the early detection of peripheral neuropathy in children and young adults with T1DM. In the present study the researchers will attempt to investigate the role of biomarkers with targeted proteomic analysis in the plasma of children with DT1 in combination with an electrophysiological study, which includes a nerve conduction study, to detect early diabetic peripheral neuropathy, before the appearance of clinical manifestations.

Eligibility Criteria

Inclusion Criteria: 1. Children with confirmed DT1 under insulin substitution therapy 2. Age 5-10 years 3. Good glycemic control with HbA1c ≤ 7.0% 4. Prepubertal patients 5. Absence of other diseases 6. Signed informed consent of the parents or guardians of patients Exclusion Criteria: 1. Presence of organic cause for neuropathy 2. Presence of other chronic disease 3. Poor glycemic control 3\. Medication

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