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Trials / Enrolling By Invitation

Enrolling By InvitationNCT07122180

Post-Market Clinical Follow-Up of the CT3 Series Continuous Glucose Monitoring System: A 14-Day Observational Study Assessing Accuracy, Safety, and Glucose Control in Patients With Type 1 and Type 2 Diabetes Mellitus

Status
Enrolling By Invitation
Phase
Study type
Observational
Enrollment
72 (estimated)
Sponsor
MDCECRO LLC · Network
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Post market Clinical follow-up of the CT3 Series Continuous Glucose Monitoring System: A 14-Day Observational Study Assessing Accuracy, Safety, and Glucose Control in patients with Type 1 and Type 2 Diabetes Mellitus

Detailed description

To re-assess the benefits of CT3 series CGM and the risks of skin abnormalities, hypoglycaemia, hyperglycaemia so as to improve CT3 series CGM continuously.

Conditions

Interventions

TypeNameDescription
DEVICECT3 Series Continuous Glucose Monitoring System:The CT3 Series CGM System is a real-time, continuous glucose monitoring device indicated for the management of diabetes in adults (age≥18 years). Interpretation of the CT3 Series CGM System results should be based on the glucose trends and several sequential readings over time. The CT3 Series CGM System also aids in the detection of episodes of hyperglycaemia and hypoglycaemia. It is intended for single-patient use. It is intended to replace fingerstick blood glucose testing for diabetes treatment decisions unless otherwise indicated

Timeline

Start date
2025-06-04
Primary completion
2025-09-17
Completion
2026-01-31
First posted
2025-08-14
Last updated
2025-08-22

Locations

1 site across 1 country: Latvia

Source: ClinicalTrials.gov record NCT07122180. Inclusion in this directory is not an endorsement.