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Checking Glucose Sensor Accuracy During Surgery in Young People With Type 1 Diabetes

Checks how accurately glucose sensors read blood sugar in young people with type 1 diabetes.

Plain-language title generated from the registry record
Registry title: Accuracy of Continuous Glucose Monitors During the Perioperative Period in Youth With Type 1 Diabetes

Key facts

Where
Aurora, United StatesSee the site

Could this be for you?

Answer for yourself. This is not a decision: only the study team can say whether you can take part.

  • Are you between 2 and 26 years old?

Source: NCT06575842, who can take part

Where in United States

  • Barbara Davis CenterAurora, United StatesTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
Print a page for my doctor

Trial details

Who runs it
University of Colorado, Denver
Trial code
NCT06575842
Record updated
12 June 2026
Original description
This study is assessing the accuracy of continuous glucose monitors during surgical procedures requiring anesthesia.Read full original descriptionShow less

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

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

Inclusion: Participants will be 2 to 26 years of age at the time of enrollment; Participants will have a diagnosis of type 1 diabetes on insulin therapy and requiring close glucose monitoring during the hospitalization and the perioperative period; 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.

Exclusion: Currently using hydroxyurea; A condition that the investigator determines would prevent the patient from participation; Pregnancy.

ClinicalTrials.gov NCT06575842