Registry of patients with diabetes and those at risk of developing it

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This project aims to create a comprehensive registry of patients diagnosed with diabetes, those at high risk of developing diabetes, and a control group of normoglycemic individuals. Participants will undergo a detailed medical interview and provide biological samples for various omics analyses, which will be evaluated using artificial intelligence algorithms. The findings will lead to new care recommendations tailored for high-risk patients and those already suffering from diabetes. The study will be conducted at the Clinical Research Center of the Medical University of Bialystok.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* patients with diagnosed diabetes (according to the American Diabetes Association criteria) - diabetes group
* patients with diagnosed prediabetes (IFG and/or IGT) - prediabetes group
* patients with normoglycemia (NFG and NGT) - normoglycemia group
* informed consent

Exclusion Criteria:

* drug addiction
* severe psychiatric disorders
* patients with gestational diabetes mellitus
* patients unable to give informed consent, legally incompetent or incapable to comply with the study terms and conditions

Where it's running

• Clinical Research Centre, Medical University of Bialystok
  Bialystok, Podlaskie Voivodeship, Poland Recruiting

Study contacts

• Study coordinator: Lukasz Szczerbinski, MD, PhD
• Email: lukasz.szczerbinski@umb.edu.pl
• Phone: +48858318150

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.