Inpatient Use of Personal Continuous Glucose Monitor (CGM) to Improve Diabetes Mellitus Control
NCT07006480 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150
Last updated 2025-10-22
Summary
The purpose of this research is to prove that data generated by your real-time personal continuous glucose monitors CGMs brought in the hospital at the time of hospitalization can be monitored and safely used to guide insulin therapy aiming to improve glycemic control and to diminish the hypoglycemia and hyperglycemia episodes without negatively affecting patients' satisfaction, providers and your nurses satisfaction with how glucose is monitored and treated in the hospital.
Conditions
Interventions
- DEVICE
-
Real time CGM data monitoring
CGM data will be monitored in real time during daytime in the hospital. Alerts about high and low glucose levels will be communicated to patient's nurse and treating providers.
- DEVICE
-
Insulin dose adjustment based on glucometer and CGM glucose data trends
Insulin dose will be modulate based on glucometer values and previous day glucose trends as recorded on CGM.
- DEVICE
-
Share CGM data on admission and on discharge from the hospital
Record 14 days' worth of CGM data prior to admission and all CGM data recorded during the hospitalization at the time of discharge from the hospital
Sponsors & Collaborators
- lead OTHER
Principal Investigators
-
Adrian G Dumitrascu, MD · Mayo Clinic
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-10-01
- Primary Completion
- 2026-06-14
- Completion
- 2026-06-14
- FDA Device
- Yes
Countries
- United States
Study Locations
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