Not medical advice. This website is not medical advice, a diagnosis, a match to a trial, or a recommendation to join a study. Listings are plain-English rewrites of public ClinicalTrials.gov records. Whether a site is still enrolling, and whether you qualify, can only be confirmed by the study team and your clinician. Source registry: ClinicalTrials.gov. Editorial rules: methodology.
RecruitingNot a traditional drug phaseinterventionalRules rewrite

Not a traditional drug phase: Continuous glucose monitoring for Type 2 Diabetes

The aim of the study is to assess the influence of continuous glucose monitoring (CGM) systems on metabolic control and quality of life in people with type 2 diabetes and overweight/obesity who are not treated with insulin. Additionally, the study aims to assess the association between metabolic control of diabetes and markers of early cardiovascular disease, taking into account the impact of CGM use.

Official registry: https://clinicaltrials.gov/study/NCT07919236 · Medical University of Bialystok · enrollment listed as 50

What this phase means

This study does not use the classic phase 1–4 drug ladder. It may be a device, a behavior program, a surgery timing study, or an early feasibility test.

Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

What the registry says happens

If you join, the listed intervention(s) are Continuous glucose monitoring, or Self-monitoring of blood glucose. The registry lists allocation as randomized. The aim of the study is to assess the influence of continuous glucose monitoring (CGM) systems on metabolic control and quality of life in people with type 2 diabetes and overweight/obesity who are not treated with insulin.

They plan to enroll about 50 people at Bialystok. Taking part typically means using or being fitted with a device plus check-ins.

Official title (unrewritten)

Continuous Glucose Monitoring Systems in People With Type 2 Diabetes Not Treated With Insulin - the Association With Metabolic Control of Diabetes and Markers of Early Vascular Changes

Interventions: Continuous glucose monitoring, Self-monitoring of blood glucose

Primary outcome (registry wording): Change in time in range

Who it is for (from inclusion criteria)

  • Ages 18 Years to 65 Years
  • Age between 18 and 65 years (both inclusive)
  • Type 2 diabetes diagnosed at least 6 months prior to entering the study
  • Body mass index ≥25 kg/m2
  • Diabetes treated with oral medications and/or GLP-1 receptor agonists and/or tirzepatide
  • No modifications of diabetes treatment in the previous 3 months
  • HbA1c between 7.5% and 10% (both inclusive)

Public study contact (from the registry)

Anna Krentowska, MD, PhD

+48858317761

anna.krentowska@umb.edu.pl

Published on ClinicalTrials.gov. Contact them as a possible participant. They decide eligibility.

Sites listed on ClinicalTrials.gov

1 listed

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FAQ about this NCT record

Is NCT07919236 still recruiting?

The sponsor posted status “Recruiting” on ClinicalTrials.gov at last ingest. Sites can pause independently. Confirm with the official record and the listed contact.

What phase is NCT07919236?

Not a traditional drug phase. Phase labels are FDA/ICH categories applied to the registry Phase field. They are not a finding that this study succeeded.

Can PlainTrials tell me if I qualify for NCT07919236?

No. The inclusion and exclusion lists on this page are readable extracts of the public eligibility block. Only the study team can screen you.

How to read a ClinicalTrials.gov record · Questions to ask the coordinator · Glossary