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Remote Continues Glucose Monitoring During the COVID-19 Pandemic in Quarantined Hospitalized Patients (CGM-ISO)

Primary Purpose

Diabetes, Covid-19, Infection

Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
Dexcom G6
Sponsored by
Nordsjaellands Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Diabetes focused on measuring endocrinology, diabetes, quarentine, isolation, CGM

Eligibility Criteria

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

Inclusion Criteria:

  1. Hospitalized with confirmed COVID-19 infection by real-time PCR or another validated method OR hospitalized with a non-COVID-19 diagnosis AND in isolation at time of inclusion.
  2. A documented clinically relevant history of diabetes or newly discovered during hospitalization.
  3. Written informed consent obtained before any trial related procedures are performed.
  4. Male or female aged over 18 years of age.
  5. Must be able to communicate with the study personnel.
  6. The subject must be willing and able to comply with trial protocol.

Exclusion Criteria:

1. Known hypersensitivity to the band-aid of the Dexcom G6 sensors

Sites / Locations

  • Nordsjællands HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

Fingerprick glucose

Open continous glucose monitoring (CGM)

Arm Description

Standard care with fingerprick glucose + blinded CGM stratification on COVID-19 status

Standard care with fingerprick glucose + un-blinded CGM stratification on COVID-19 status

Outcomes

Primary Outcome Measures

Time In Range (TIR) for blood glucose
TIR is presented in percent of time in which the participants' glucose values are in different glucose ranges.

Secondary Outcome Measures

Saved patient-personnel contacts related to blood glucose measurements.
Saved patient-personnel contacts related to blood glucose measurements, incl. time healthcare providers spent on diabetes related tasks and PPE related tasks, during the patients' hospitalization.
Glucose variations during hospitalization
Additional glucose outcomes based on data from Dexcom G6 are for example Time Above Range (TAR), Time Below Range (TBR), average glucose, variance in glucose (CV), etc.
Blood glucose lowering interventions
That is: Tablet-based and insulin-based regimens and number of times that sliding scale insulin (including dose of insulin) has been administered for each patient.
CGM sensor performance
Number of techincal errors during the sensors lifetime.
Course of hospital stay.
Hospital death (yes/no), length of stay at hospital, need for respiratory support (yes/no) and intensive care (yes/no), recovered vs. fatal (death within 60 days from admission).

Full Information

First Posted
May 26, 2020
Last Updated
June 11, 2020
Sponsor
Nordsjaellands Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04430608
Brief Title
Remote Continues Glucose Monitoring During the COVID-19 Pandemic in Quarantined Hospitalized Patients
Acronym
CGM-ISO
Official Title
Remote Glucose Monitoring of Patients With Diabetes Quarantined During the COVID-19 Pandemic - a Hospital-Based Randomized Controlled Trial of the Effect of Remote Continuous Glucose Monitoring Compared to Usual Glucose Monitoring
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Unknown status
Study Start Date
May 25, 2020 (Actual)
Primary Completion Date
April 25, 2021 (Anticipated)
Study Completion Date
May 25, 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Nordsjaellands Hospital

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.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a randomized controlled trial of isolated patients with diabetes admitted to Nordsjællands Hospital with or without COVID-19-pneumonia. A continuous glucose monitoring (CGM) based system with transmission of glucose data to a central system is used for remote monitoring of glucose levels and compared to standard finger-prick glucose. Blinded (to patients) CGM is mounted in the finger-prick group.
Detailed Description
Epidemics and pandemics are a constant threat to health care systems globally. This stresses the importance of preparedness for a large amount of hospitalized quarantined patients in isolation, with the extra challenges it brings. The COVID-19 pandemic challenges the Danish health care system in many aspects: An increased number of citizens are expected to be admitted to hospital due to COVID-19 infected pneumonia and this will demand extra workforce resources, extra use of protective equipment (gowns, masks, gloves, etc) and extra time used for taking protective equipment on and off. In concert these extra demands will drain the health care system and any initiative to reduce these challenges is needed. In this randomized controlled trial, isolated patients with diabetes will be randomized to either standard care fingerprick glucose + blinded CGM or Dexcom G6 only.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes, Covid-19, Infection
Keywords
endocrinology, diabetes, quarentine, isolation, CGM

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients are randomized 1:1 to either CGM or Fingerprick group
Masking
None (Open Label)
Allocation
Randomized
Enrollment
72 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Fingerprick glucose
Arm Type
Other
Arm Description
Standard care with fingerprick glucose + blinded CGM stratification on COVID-19 status
Arm Title
Open continous glucose monitoring (CGM)
Arm Type
Experimental
Arm Description
Standard care with fingerprick glucose + un-blinded CGM stratification on COVID-19 status
Intervention Type
Device
Intervention Name(s)
Dexcom G6
Intervention Description
The investigational device is a CGM Dexcom G6. The Dexcom G6 System is intended to replace fingerstick blood glucose testing for diabetes treatment decisions. The device-system consists of a sensor, the Dexcom G6 device/sender, and connects to a smart device like a cellphone. The Dexcom G6 CGM system is probably the most precise system on the market and with no need for daily calibration with finger prick glucose. The Dexcom G6 sensor can last for 10 days without calibration and is approved for diabetes treatment decision making. Dexcom G6 has been extensively tested and is safe and approved even for pregnant women. The CE Marking confirms that the G6 system meets the Essential Requirements of the Medical Device Directive MDD 93/42/EEC as amended by 2007/47/EC.
Primary Outcome Measure Information:
Title
Time In Range (TIR) for blood glucose
Description
TIR is presented in percent of time in which the participants' glucose values are in different glucose ranges.
Time Frame
1-2 weeks
Secondary Outcome Measure Information:
Title
Saved patient-personnel contacts related to blood glucose measurements.
Description
Saved patient-personnel contacts related to blood glucose measurements, incl. time healthcare providers spent on diabetes related tasks and PPE related tasks, during the patients' hospitalization.
Time Frame
1-2 weeks
Title
Glucose variations during hospitalization
Description
Additional glucose outcomes based on data from Dexcom G6 are for example Time Above Range (TAR), Time Below Range (TBR), average glucose, variance in glucose (CV), etc.
Time Frame
1-2 weeks
Title
Blood glucose lowering interventions
Description
That is: Tablet-based and insulin-based regimens and number of times that sliding scale insulin (including dose of insulin) has been administered for each patient.
Time Frame
1-2 weeks
Title
CGM sensor performance
Description
Number of techincal errors during the sensors lifetime.
Time Frame
1-2 weeks
Title
Course of hospital stay.
Description
Hospital death (yes/no), length of stay at hospital, need for respiratory support (yes/no) and intensive care (yes/no), recovered vs. fatal (death within 60 days from admission).
Time Frame
1-2 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Hospitalized with confirmed COVID-19 infection by real-time PCR or another validated method OR hospitalized with a non-COVID-19 diagnosis AND in isolation at time of inclusion. A documented clinically relevant history of diabetes or newly discovered during hospitalization. Written informed consent obtained before any trial related procedures are performed. Male or female aged over 18 years of age. Must be able to communicate with the study personnel. The subject must be willing and able to comply with trial protocol. Exclusion Criteria: 1. Known hypersensitivity to the band-aid of the Dexcom G6 sensors
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carina Klarskov, MD
Phone
004548294829
Email
carina.kirstine.klarskov@regionh.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Peter L. Kristensen, MD, ph.D
Phone
004548294829
Email
peter.lommer.kristensen.01@regionh.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter L. Kristensen, MD, ph.D
Organizational Affiliation
Nordsjællands Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nordsjællands Hospital
City
Hillerød
ZIP/Postal Code
3400
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Peter L. Kristensen, MD, ph.D
Phone
004548294829
Email
peter.lommer.kristensen.01@regionh.dk
First Name & Middle Initial & Last Name & Degree
Carina Klarskov, MD
Phone
004548284829
Email
carina.kirstine.klarskov@regionh.dk

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Undecided, will be updated
Citations:
PubMed Identifier
34524009
Citation
Klarskov CK, Windum NA, Olsen MT, Dungu AM, Jensen AK, Lindegaard B, Pedersen-Bjergaard U, Kristensen PL. Telemetric Continuous Glucose Monitoring During the COVID-19 Pandemic in Isolated Hospitalized Patients in Denmark: A Randomized Controlled Exploratory Trial. Diabetes Technol Ther. 2022 Feb;24(2):102-112. doi: 10.1089/dia.2021.0291. Epub 2022 Jan 4.
Results Reference
derived
PubMed Identifier
33239100
Citation
Klarskov CK, Lindegaard B, Pedersen-Bjergaard U, Kristensen PL. Remote continuous glucose monitoring during the COVID-19 pandemic in quarantined hospitalized patients in Denmark: A structured summary of a study protocol for a randomized controlled trial. Trials. 2020 Nov 25;21(1):968. doi: 10.1186/s13063-020-04872-4.
Results Reference
derived

Learn more about this trial

Remote Continues Glucose Monitoring During the COVID-19 Pandemic in Quarantined Hospitalized Patients

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