Study S002508

Prospective Post-market Clinical Follow-up (PMCF) Study Aimed to Evaluate the Change in Glucometric Parameters in Adult Patients With Type 1 or Type 2 DiabETes From Europe Using the iCan o3 CGM SysTem for a 60-day Period

ClinicalTrials.gov record

Registration

Registration: NCT06904846
Acronym: DETECT
Study type: INTERVENTIONAL
Masking: NONE
Status: ENROLLING_BY_INVITATION
Enrollment: 70
Start: 2025-04-23
Primary completion: 2026-04-30
Lead sponsor: Sinocare
Conditions: Diabetes Mellitus; Continuous Glucose Monitoring System
Interventions: DEVICE:iCan o3 CGM Continuous Glucose Monitoring System
Results posted: FALSE
Individual participant data sharing: NO

Registered primary outcomes

Improvement of Glycemic control [60 days]

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