Continuous Glucose Monitoring in Dialysis Patients to Overcome Dysglycemia Trial

Description

This randomized controlled trial will investigate whether use of continuous glucose monitoring (CGM) vs. usual care with self-monitored blood glucose 1) enhances glycemic control, 2) reduces hypoglycemia risk, and 3) improves quality of life, diabetes distress, and fear of hypoglycemia in hemodialysis patients with diabetes mellitus.

Conditions

Hemodialysis, Diabete Mellitus, Continuous Glucose Monitoring

Study Overview

Study Details

Study overview

This randomized controlled trial will investigate whether use of continuous glucose monitoring (CGM) vs. usual care with self-monitored blood glucose 1) enhances glycemic control, 2) reduces hypoglycemia risk, and 3) improves quality of life, diabetes distress, and fear of hypoglycemia in hemodialysis patients with diabetes mellitus.

Continuous Glucose Monitoring in Dialysis Patients to Overcome Dysglycemia Trial

Continuous Glucose Monitoring in Dialysis Patients to Overcome Dysglycemia Trial

Condition
Hemodialysis
Intervention / Treatment

-

Contacts and Locations

Orange

University of California, Irvine, Orange, California, United States, 92868

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Ability to provide written informed consent
  • * Age ≥18 years old
  • * End-stage kidney disease status receiving in-center hemodialysis ≥4 weeks
  • * Type 1 or type 2 diabetes
  • * Actively performing self-monitored blood glucose (SMBG) testing for ≥4 weeks
  • * ≥70% compliance wearing continuous glucose monitoring (CGM) device during the pre-trial period
  • * Inability to provide informed consent or comply with the study protocol
  • * Limited visual acuity
  • * Inability to wear CGM device
  • * Prior use of CGM
  • * Active pregnancy or planning a pregnancy

Ages Eligible for Study

18 Years to 99 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of California, Irvine,

Study Record Dates

2026-01-31