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Accuracy of CGM in the ICU, Compared to Standard of Care

University of British Columbia logo

University of British Columbia

Status

Unknown

Conditions

Diabetes

Treatments

Device: Continuous Glucose Sensor

Study type

Observational

Funder types

Other
Industry

Identifiers

NCT04352907
H19-02392

Details and patient eligibility

About

To determine the performance of the Dexcom CGM device in comparison to arterial glucose samples.

Full description

The performance of the Dexcom continuous glucose sensor will be compared with the current standard of care which is arterial glucose samples analyzed on a glucose meter. Subjects will be ICU patients receiving intravenous insulin infusions.

Enrollment

20 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • minimum age 18 years
  • anticipated to be on an insulin infusion for 3-7 consecutive days
  • 10 of these subjects will be on vasopressors who will be receiving large volume fluid resuscitation

Exclusion criteria

  • subjects not on insulin infusion

Trial contacts and locations

1

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Central trial contact

David M Thompson, MD; Barbara J Allan, MHA

Data sourced from clinicaltrials.gov

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