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Clinical Trial Details — Status: Recruiting

Administrative data

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

Study information

Verified date March 2024
Source Mayo Clinic
Contact Sarah Schettle, PA-C
Phone (507) 293-1375
Email Schettle.Sarah@mayo.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

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

Study Design


Intervention

Device:
Freestyle Libre 3 Continuous Glucose Monitor (CGM)
Subjects will be provided a Freestyle Libre 3 CGM for monitoring of blood glucose levels throughout participation in the study (approximately 3 months). CGM data will be uploaded to the LibreLink app on a weekly basis for review of glucose control and consultation with a diabetes-trained provider for any values outside of normal ranges. Adjustments to diet and medication therapy (antihyperglycemic therapy) will be made during consultations to improve episodes of hypoglycemia or severe hyperglycemia that were observed.

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

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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