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Clinical Trial Summary

The investigators believe that addition of real time continuous glucose monitoring (RT-CGM) improves glycemic outcome in patients with Type 2 diabetes compared to self-monitored blood glucose (SMBG), for patients who are not at target A1C regardless of treatment modality. The investigators aims to assess glycemic and quality of life (QoL) benefits of adding and using RT-CGM patients with Type 2 Diabetes Mellitus (T2DM), not at their A1C goal and relying on SMBG for diabetes-management decisions.


Clinical Trial Description

Prescreened and eligible subjects will obtain CGM and basic CGM education upon enrollment. They will initially be given three months of CGM supplies and return to the study center every 3 months for more supplies. In addition, baseline data and labs will be collected at visits. All subjects will return to the clinic after every three months for assessment and assignment of three more months of CGM supplies. This will repeat for a 12 month period. Patient reported outcome (PRO) measurements will be obtained at the beginning and end of the study. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05351190
Study type Interventional
Source Blanchard Valley Health System
Contact
Status Enrolling by invitation
Phase N/A
Start date May 15, 2022
Completion date December 31, 2024

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