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NCT05933161Recruiting

A Study of Glycemic Control in Left Ventricular Assist

GLYcemic Control Evaluation by Continuous Glucose Monitor Compared With a1C in Left Ventricular Assist Device-supported Patients (GLYCEM1C-LVAD)

Source: ClinicalTrials.gov · Last updated 8 May 2026

Brief summary (registry, in English)

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 (registry)
Recruiting
Study type
Observational
Enrollment
20 (estimated)
First submitted
28 Jun 2023
Start date
10 Nov 2023
Primary completion date
30 Apr 2027
Lead sponsor
Mayo Clinic
NCT number
NCT05933161

What you commit to

  • Study type: Observational
  • Planned participants: 20
  • From 10 Nov 2023 to the primary completion date, 30 Apr 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Type I diabetics
  • Unable to return at 3 month evaluation
  • Unwillingness to participate

Who the study is looking for

  • 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mayo Clinic in Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.