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NOT YET RECRUITING
NCT06471699
NA

The Effect of Continuous Glucose Monitoring in Individuals With Newly Diagnosed Type 2 Diabetes

Sponsor: Vastra Gotaland Region

View on ClinicalTrials.gov

Summary

The aim of the current study is to evaluate effectiveness, sustainability and satisfaction of CGM in adult persons with newly diagnosed type 2 diabetes. The study is a randomized clinical trial randomizing patients to CGM or SMBG over 26 weeks with a follow-up period up to 70 weeks. An extension period will exist between 26 and 70 weeks. Between 26-52 weeks both groups will use only capillary testing for glucose monitoring and during 53-70 weeks the group initially randomized to capillary testing will use CGM. During the extension period similar variables will be evaluated as during the main phase of the trial including HbA1c, CGM-metrics, glucose-lowering medications, physical activity, treatment satisfaction and well-being.

Official title: A Randomized Trial of the Effect of Continuous Glucose Monitoring (CGM) in Individuals With Newly Diagnosed Type 2 Diabetes

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

250

Start Date

2024-11-01

Completion Date

2030-12-31

Last Updated

2024-06-24

Healthy Volunteers

No

Conditions

Interventions

DEVICE

Continous Glucose Monitoring

The aim is to examine if the use of CGM will give the participants a significant support to implement lifestyle improvements in individuals with new on-set type 2 diabetes

OTHER

Self monitoring blood glucose

Capillary testing as in standard procedure