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Continuous Glucose Monitor
Continuous Glucose Monitor (CGM) for Diabetes
N/A
Waitlist Available
Led By Adrian Dumitrascu, MD
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up from date of enrollment and until discharge from the hospital up to 30 days.
Awards & highlights
Study Summary
This study is evaluating whether continuous glucose monitors are accurate for blood glucose monitoring.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ from date of enrollment and until discharge from the hospital up to 30 days.
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~from date of enrollment and until discharge from the hospital up to 30 days.
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
CGM accuracy
Secondary outcome measures
CGM recorded hyperglycemia episodes
CGM recorded hypoglycemia episodes
Trial Design
1Treatment groups
Experimental Treatment
Group I: CGM PatientsExperimental Treatment1 Intervention
Subjects with diabetes mellitus or medication induced diabetes that have been admitted to the hospital after a surgery for organ transplantation or scheduled for organ transplant surgery will be fitted with a CGM monitor to monitor glucose levels during hospitalization
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Continuous Glucose Monitor (CGM)
2017
Completed Phase 3
~650
Find a Location
Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,212 Previous Clinical Trials
3,766,988 Total Patients Enrolled
22 Trials studying Diabetes
6,803 Patients Enrolled for Diabetes
Adrian Dumitrascu, MDPrincipal InvestigatorMayo Clinic
3 Previous Clinical Trials
270 Total Patients Enrolled
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