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Remote Glucose Monitoring System in Hospitalized Patients With Diabetic Ketoacidosis (DKA)

Primary Purpose

Diabetic Ketoacidosis

Status
Not yet recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
DEXCOM G6 CGM
Sponsored by
Columbia University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Diabetic Ketoacidosis focused on measuring Continuous Glucose Monitoring, Diabetes, Hospitalized patients

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age >18 years
  • AG>20 mEq/L
  • Bicarbonate <15mEq/L
  • Positive urine ketones or beta hydroxybutyrate >0.3 mmol/L

Exclusion Criteria:

  • Hypotension (Blood Pressure below 80/60 mmHg)
  • Requirement for pressor therapy
  • Contraindication for utilizing Dexcom CGM

Sites / Locations

  • New York Presbyterian Hospital/ Columbia University Irving Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

DEXCOM G6 CGM

Hourly Finger Stick Point of Care (Historical Control)

Arm Description

Continuous glucose monitoring by DEXCOM G6 (glucose monitoring device) in a step-down unit in participants with DKA

Retrospective chart review of DKA patients that received hourly glucose monitoring by finger stick while in the ICU

Outcomes

Primary Outcome Measures

Time to Resolution of Metabolic Acidosis
Time to resolution of metabolic acidosis measured in hours. Resolution defined as anion gap (AG) <17 mEq/L and bicarbonate >19 mEq/L.

Secondary Outcome Measures

Length of ICU Stay
Length of ICU stay measured in days
Length of Hospital Stay
Length of hospital stay measured days
Number of Hypoglycemic Events
The number of hypoglycemic events will be recorded. A hypoglycemic event is defined as glucose level <70 mg/dL.
Cost savings
Cost savings calculated by comparison of cost when non-critically DKA participants have glucose levels monitored via CGM and treated in the stepdown unit compared to participants who have glucose levels monitored via hourly fingersticks and treated in the ICU.

Full Information

First Posted
June 26, 2022
Last Updated
June 26, 2022
Sponsor
Columbia University
Collaborators
DexCom, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT05439928
Brief Title
Remote Glucose Monitoring System in Hospitalized Patients With Diabetic Ketoacidosis (DKA)
Official Title
Remote Glucose Monitoring Using the Dexcom G6 Continuous Glucose Monitoring (CGM) System in Hospitalized Patients With Diabetic Ketoacidosis (DKA)
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
July 2022 (Anticipated)
Primary Completion Date
July 2023 (Anticipated)
Study Completion Date
July 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Columbia University
Collaborators
DexCom, Inc.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this research study is to investigate the use of continuous glucose monitoring (CGM) device DEXCOM G6 in non-critically patients treated for diabetic emergency such as diabetic ketoacidosis (DKA). Patients who have DKA require hourly monitoring of glucose (sugar) level which traditionally requires admission to the intensive care unit (ICU) for hourly fingerstick monitoring. With the use of CGM device, in this research study hourly fingerstick monitoring is replaced by continuous glucose monitor (CGM) which provides glucose levels continuously in real time for nurses and provider. The investigators are testing to see if in the future patients can be treated in the stepdown unit (an intermediate care level between the intensive care unit and the general medical unit) if they do not require higher level of care besides hourly glucose monitoring. Continuous glucose monitoring (CGM) device DEXCOM G6 currently FDA Approved for patients with diabetes and is widely used for glucose monitoring in patients with diabetes in the outpatient setting. The investigators want to study the use of the DEXCOM G6 CGM in the inpatient setting to monitoring glucose levels remotely in the treatment of diabetic emergencies such as diabetic ketoacidosis and compare their care to those receiving hourly fingerstick glucose monitoring in the ICU.
Detailed Description
During the height of the COVID-19 pandemic, the investigators launched a quality improvement project with the goal of treating non-critically ill DKA patients outside of ICU setting to reallocate ICU beds for critically ill patients. The standard of care is for DKA patients to be treated in the ICU setting because the DKA protocol requires hourly fingerstick glucose monitoring, which is considered higher level of care and not appropriate for stepdown unit or medical/surgical wards. During this quality improvement project, the investigators monitored glucose levels remotely with continuous glucose monitoring (CGM) device DEXCOM G6, eliminating the need for hourly fingerstick glucose testing. Therefore, patients with DKA whose glucose levels were monitored with DEXCOM G6 CGM were treated in the stepdown unit instead of the ICU setting. Once the number of COVID cases decreased and ICU beds were more readily available, the hospital returned to practicing pre-COVID standard of care, which was admitting DKA patient to the ICU for hourly glucose monitoring. This study is a combined retrospective and prospective study of DKA patients. The investigators propose a retrospective chart review of DKA patients who had glucose levels monitored with DEXCOM G6 CGM during the COVID-19 pandemic. In the prospective portion of this study, participants will be enrolled and will undergo continuous glucose monitoring with DEXCOM G6 instead of the hourly fingerstick point of care glucose testing. Data collected for participants monitored via DEXCOM G6 (retrospective and prospective study data combined analysis) will be compared to participants with glucose levels monitored via hourly fingerstick in the ICU setting.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Ketoacidosis
Keywords
Continuous Glucose Monitoring, Diabetes, Hospitalized patients

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
98 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
DEXCOM G6 CGM
Arm Type
Experimental
Arm Description
Continuous glucose monitoring by DEXCOM G6 (glucose monitoring device) in a step-down unit in participants with DKA
Arm Title
Hourly Finger Stick Point of Care (Historical Control)
Arm Type
No Intervention
Arm Description
Retrospective chart review of DKA patients that received hourly glucose monitoring by finger stick while in the ICU
Intervention Type
Device
Intervention Name(s)
DEXCOM G6 CGM
Intervention Description
Continuous glucose monitoring
Primary Outcome Measure Information:
Title
Time to Resolution of Metabolic Acidosis
Description
Time to resolution of metabolic acidosis measured in hours. Resolution defined as anion gap (AG) <17 mEq/L and bicarbonate >19 mEq/L.
Time Frame
Up to 10 days
Secondary Outcome Measure Information:
Title
Length of ICU Stay
Description
Length of ICU stay measured in days
Time Frame
Up to 20 days
Title
Length of Hospital Stay
Description
Length of hospital stay measured days
Time Frame
Up to 20 days
Title
Number of Hypoglycemic Events
Description
The number of hypoglycemic events will be recorded. A hypoglycemic event is defined as glucose level <70 mg/dL.
Time Frame
Up to 20 days
Title
Cost savings
Description
Cost savings calculated by comparison of cost when non-critically DKA participants have glucose levels monitored via CGM and treated in the stepdown unit compared to participants who have glucose levels monitored via hourly fingersticks and treated in the ICU.
Time Frame
Up to 20 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >18 years AG>20 mEq/L Bicarbonate <15mEq/L Positive urine ketones or beta hydroxybutyrate >0.3 mmol/L Exclusion Criteria: Hypotension (Blood Pressure below 80/60 mmHg) Requirement for pressor therapy Contraindication for utilizing Dexcom CGM
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Magdalena Bogun, MD
Phone
2128515494
Email
mmb2263@cumc.columbia.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Marc Probst, MD
Phone
2123054687
Email
mp4013@cumc.columbia.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Magdalena Bogun, MD
Organizational Affiliation
Columbia University
Official's Role
Principal Investigator
Facility Information:
Facility Name
New York Presbyterian Hospital/ Columbia University Irving Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
10032
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
20799388
Citation
Juvenile Diabetes Research Foundation Continuous Glucose Monitoring Study Group. Validation of measures of satisfaction with and impact of continuous and conventional glucose monitoring. Diabetes Technol Ther. 2010 Sep;12(9):679-84. doi: 10.1089/dia.2010.0015.
Results Reference
background
PubMed Identifier
32393587
Citation
Nair BG, Dellinger EP, Flum DR, Rooke GA, Hirsch IB. A Pilot Study of the Feasibility and Accuracy of Inpatient Continuous Glucose Monitoring. Diabetes Care. 2020 Nov;43(11):e168-e169. doi: 10.2337/dc20-0670. Epub 2020 May 11. No abstract available.
Results Reference
background
PubMed Identifier
32370606
Citation
Pasquel FJ, Umpierrez GE. Individualizing Inpatient Diabetes Management During the Coronavirus Disease 2019 Pandemic. J Diabetes Sci Technol. 2020 Jul;14(4):705-707. doi: 10.1177/1932296820923045. Epub 2020 May 5.
Results Reference
background
PubMed Identifier
33435706
Citation
Chow KW, Kelly DJ, Rieff MC, Skala PA, Kravets I, Charitou MM, Morley EJ, Gupta R, Miller JD. Outcomes and Healthcare Provider Perceptions of Real-Time Continuous Glucose Monitoring (rtCGM) in Patients With Diabetes and COVID-19 Admitted to the ICU. J Diabetes Sci Technol. 2021 May;15(3):607-614. doi: 10.1177/1932296820985263. Epub 2021 Jan 12.
Results Reference
background
PubMed Identifier
31980123
Citation
Davis GM, Galindo RJ, Migdal AL, Umpierrez GE. Diabetes Technology in the Inpatient Setting for Management of Hyperglycemia. Endocrinol Metab Clin North Am. 2020 Mar;49(1):79-93. doi: 10.1016/j.ecl.2019.11.002.
Results Reference
background
PubMed Identifier
29936424
Citation
Umpierrez GE, Klonoff DC. Diabetes Technology Update: Use of Insulin Pumps and Continuous Glucose Monitoring in the Hospital. Diabetes Care. 2018 Aug;41(8):1579-1589. doi: 10.2337/dci18-0002. Epub 2018 Jun 23.
Results Reference
background
PubMed Identifier
20945468
Citation
Newton CA, Smiley D, Bode BW, Kitabchi AE, Davidson PC, Jacobs S, Steed RD, Stentz F, Peng L, Mulligan P, Freire AX, Temponi A, Umpierrez GE. A comparison study of continuous insulin infusion protocols in the medical intensive care unit: computer-guided vs. standard column-based algorithms. J Hosp Med. 2010 Oct;5(8):432-7. doi: 10.1002/jhm.816.
Results Reference
background
PubMed Identifier
32853901
Citation
Pal R, Banerjee M, Yadav U, Bhattacharjee S. Clinical profile and outcomes in COVID-19 patients with diabetic ketoacidosis: A systematic review of literature. Diabetes Metab Syndr. 2020 Nov-Dec;14(6):1563-1569. doi: 10.1016/j.dsx.2020.08.015. Epub 2020 Aug 18.
Results Reference
background
PubMed Identifier
32314455
Citation
Li J, Wang X, Chen J, Zuo X, Zhang H, Deng A. COVID-19 infection may cause ketosis and ketoacidosis. Diabetes Obes Metab. 2020 Oct;22(10):1935-1941. doi: 10.1111/dom.14057. Epub 2020 May 18.
Results Reference
background
PubMed Identifier
28372715
Citation
Fayfman M, Pasquel FJ, Umpierrez GE. Management of Hyperglycemic Crises: Diabetic Ketoacidosis and Hyperglycemic Hyperosmolar State. Med Clin North Am. 2017 May;101(3):587-606. doi: 10.1016/j.mcna.2016.12.011.
Results Reference
background
PubMed Identifier
32221579
Citation
Livingston E, Desai A, Berkwits M. Sourcing Personal Protective Equipment During the COVID-19 Pandemic. JAMA. 2020 May 19;323(19):1912-1914. doi: 10.1001/jama.2020.5317. No abstract available.
Results Reference
background

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Remote Glucose Monitoring System in Hospitalized Patients With Diabetic Ketoacidosis (DKA)

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