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Accuracy of Continuous Glucose Monitors During the Perioperative Period in Youth With Type 1 Diabetes

Description

This study is assessing the accuracy of continuous glucose monitors during surgical procedures requiring anesthesia.

Conditions

Type 1 Diabetes
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Related Conditions:

Type 1 Diabetes

Study Overview

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Study Details

Study overview

This study is assessing the accuracy of continuous glucose monitors during surgical procedures requiring anesthesia.

Accuracy of Continuous Glucose Monitors During the Perioperative Period in Youth With Type 1 Diabetes

Accuracy of Continuous Glucose Monitors During the Perioperative Period in Youth With Type 1 Diabetes

Condition
Type 1 Diabetes
Intervention / Treatment

-

Contacts and Locations

Aurora

Barbara Davis Center, Aurora, Colorado, United States, 80045

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

  • 1. Participants will be 2 to 26 years of age at the time of enrollment.
  • 2. Participants will have a diagnosis of type 1 diabetes on insulin therapy and requiring close glucose monitoring during the hospitalization and the perioperative period.
  • 3. Participant currently wearing a continuous glucose monitor (for example: Dexcom G6 or G7; Freestyle Libre 2, 2 Plus, or 3; Medtronic Guardian 3 or 4; or future sensors as they become available) for home diabetes management and willing to share personal CGM data with the BDC clinical CGM account.
  • 1. Pregnancy.
  • 2. Currently using hydroxyurea.
  • 3. A condition that the investigator determines would prevent the patient from participation.

Ages Eligible for Study

2 Years to 26 Years

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Colorado, Denver,

Study Record Dates

2025-09-01