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A Pilot Study of the Feasibility and Accuracy of the TrueVie CGM System - A Non-Significant Risk Study

Continuous Glucose Monitoring Clinical Trial

Official title:
A Pilot Study of the Feasibility and Accuracy of the TrueVie Continuous Glucose Monitoring System - A Non-Significant Risk Study

Clinical Trial Summary

The purpose of the investigation is to obtain sufficient preliminary information about the performance of the TrueVie Continuous Glucose Monitoring (CGM) device to identify any need for any design modifications.

Clinical Trial Description

After being informed about the study and potential risks, all participants giving written informed consent will be screened for participation. Qualifying participants will insert CGM sensors and come to 3 clinic visits at the beginning, middle and end of the 15 days intended sensor life. At the clinic visits participants are served two meals and perform a brief period of exercise of moderate intensity while blood samples are drawn according to a planned schedule timed to coincide with the TrueVie measurements. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05348928
Study type Observational
Source Sinocare
Contact
Status Completed
Phase
Start date May 4, 2022
Completion date June 16, 2022
View Details
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