Type 2 Diabetes Mellitus Clinical Trial
— GLYCEM1C-LVADOfficial title:
GLYcemic Control Evaluation by Continuous Glucose Monitor Compared With a1C in Left Ventricular Assist Device-supported Patients (GLYCEM1C-LVAD)
NCT number | NCT05933161 |
Other study ID # | 22-011965 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | November 10, 2023 |
Est. completion date | July 2025 |
The study is being conducted to understand if the hemoglobin A1c, a measurement of control of blood sugars over a 3-month time, is valid in patients with Left Ventricular Assist Devices (LVADs) in place. To understand whether it is an adequate measurement, the investigators will compare the A1c to results from a continuous glucose monitor (CGM) measurement of blood sugars. By monitoring blood sugars continuously, the investigators will also assess whether they can get better control of blood sugars with a CGM, including avoiding low blood sugars.
Status | Recruiting |
Enrollment | 20 |
Est. completion date | July 2025 |
Est. primary completion date | April 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Prior implantation of contemporary, centrifugal flow LVAD (HeartWare or HeartMate 3) at any time after 2010 - Diagnosis of type II diabetes mellitus - Any antihyperglycemic regimen - Greater than 3 months out from LVAD implantation - Capable of utilizing smartphone device for LibreLink app for uploading glycemic data - Patients may be enrolled who have preexisting CGM in place. Exclusion Criteria: - Type I diabetics - Unable to return at 3 month evaluation - Unwillingness to participate |
Country | Name | City | State |
---|---|---|---|
United States | Mayo Clinic in Rochester | Rochester | Minnesota |
Lead Sponsor | Collaborator |
---|---|
Mayo Clinic |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Average glucose values based on continuous glucose monitoring | Average level of blood sugar reported in mg/dL obtained via the Freestyle Libre 3 CGM over a 3 month period. | 3 months | |
Primary | Estimated average glucose (eAG) values based on hemoglobin-A1c lab values | Estimated average level of blood sugar reported in mg/dL based on conversion of hemoglobin-A1c lab values (eAG=28.7*A1C - 46.7) collected at the 3-month visit. | 3 months | |
Primary | Estimated average glucose (eAG) values based on fructosamine lab values | Estimated average level of blood sugar reported in mg/dL based on conversion of fructosamine lab values (eAG= 28.7*(0.017 x fructosamine + 1.61) - 46.7) collected at the 3-month visit. | 3 months | |
Secondary | Number of adjustments of antihyperglycemic agents | Number of adjustments made to diet and medication therapy based on consultation from a trained diabetes specialist to improve episodes of hypoglycemia or severe hyperglycemia following review of glucose levels obtained via the Freestyle Libre 3 CGM. | 3 months | |
Secondary | Number of hypoglycemic unawareness episodes | Number of hypoglycemia unawareness episodes defined as periods where subjects did not know that they had low blood sugar according to Freestyle Libre 3 CGM generated alerts. | 3 months |
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