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GLYcemic Control Evaluation by Continuous Glucose Monitor Compared With a1C in Left Ventricular Assist Device-supported Patients (GLYCEM1C-LVAD)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT05933161-Jul 28, 2026
NCT ID
NCT05933161
Status
RECRUITING
Phase
Observational Study
Sponsor
Mayo Clinic
Executive brief
Investment-Ready Snapshot
The GLYCEM1C-LVAD study, sponsored by Mayo Clinic, aims to validate the use of hemoglobin A1c as a measure of glycemic control in patients with LVADs, a population that may experience unique challenges in diabetes management. The study leverages the Freestyle Libre 3 Continuous Glucose Monitor (CGM) to provide real-time glucose data, potentially leading to improved patient outcomes through better glycemic control. The findings could enhance the market positioning of CGM devices in specialized patient populations, indicating a growing need for tailored diabetes management solutions. The study's outcomes may influence future guidelines and reimbursement policies, thereby impacting market dynamics and competitive positioning among diabetes management technologies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05933161
Indication
Type 2 Diabetes Mellitus
Modality
medical device
Target
Continuous Glucose Monitoring in Type 2 Diabetes Mellitus patients with Left Ventricular Assist Devices (LVADs)
Intervention
Freestyle Libre 3 Continuous Glucose Monitor (CGM)
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.