DEXCOM-HD: Dexcom G6 Continuous Glucose Monitoring in Hemodialysis

Sponsor
University of California, Irvine (Other)
Overall Status
Recruiting
CT.gov ID
NCT04217161
Collaborator
DexCom, Inc. (Industry)
30
1
1
22.7
1.3

Study Details

Study Description

Brief Summary

This is a pilot study enrolling adult hemodialysis patients with diabetes recruited from the University of California Irvine Medical Center (UCIMC) who will undergo simultaneous measurement of glucose levels using 1) continuous glucose monitor (CGM) measured by a Dexcom G6 device vs. 2) "gold-standard" blood glucose levels using capillary fingerstick or venous blood glucose measurements obtained on a point of care (POC) blood glucose meter. The study will assess Dexcom G6 accuracy by comparing glucose levels on the CGM device vs. blood glucose measurements in the study population.

Condition or Disease Intervention/Treatment Phase
  • Device: Dexcom G6 Continuous Glucose Monitor
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Comparison of Dexcom G6 Continuous Glucose Monitoring System and Blood Glucose Levels in Adult Hemodialysis Patients With Diabetes
Actual Study Start Date :
Mar 1, 2020
Anticipated Primary Completion Date :
Jan 21, 2022
Anticipated Study Completion Date :
Jan 21, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Dexcom G6 Continuous Glucose Monitor

Device: Dexcom G6 Continuous Glucose Monitor
Eligible patients will undergo DDexcom G6 Continuous Glucose Monitor device placement

Outcome Measures

Primary Outcome Measures

  1. Blood glucose measurement [3 to 5 days]

    Proportion of CGM values within 20% of blood glucose levels >100 mg/dl or within 20 mg/dl of blood glucose level for levels <=100 mg/dl. (Will examine different thresholds of CGM values within a certain range of blood glucose levels, i.e., 10%, 15%, 25%.)

Secondary Outcome Measures

  1. Hypoglycemia events [3 to 5 days]

    Comparison in number of hypoglycemia events (glucose <70 mg/dl) determined by CGM or by blood glucose measurements

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adult hemodialysis patients age 18 years or older

  • Have a comorbidity of diabetes

  • Receipt of care from the inpatient University of California Irvine Medical Center nephrology consult service

  • Expected hospital stay ≥48 hours

  • Have the ability to directly provide informed consent for participation in the study

Exclusion Criteria:
  • Critically-ill patients receiving care in the intensive care unit (ICU) or cardiac care unit (CCU)

  • Moribund patients expected to die within 48 hours

  • Presence of any condition deemed by PI's judgment that would seriously limit life expectancy (i.e., poor survival)

  • Pregnant

  • Unwilling or unable to provide informed consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of California Irvine Orange California United States 92868

Sponsors and Collaborators

  • University of California, Irvine
  • DexCom, Inc.

Investigators

  • Principal Investigator: Connie Rhee, MD, MSc, Faculty

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University of California, Irvine
ClinicalTrials.gov Identifier:
NCT04217161
Other Study ID Numbers:
  • HS# 2019-5585
First Posted:
Jan 3, 2020
Last Update Posted:
Jun 15, 2021
Last Verified:
Jun 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Jun 15, 2021