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Accuracy of Continuous Glucose Monitors During the Perioperative Period in Youth With Type 1 Diabetes
RecruitingObservational study
Who can join
Ages 2 to 26 · All sexes
Full eligibility criteria
Inclusion 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. Exclusion Criteria: 1. Pregnancy. 2. Currently using hydroxyurea. 3. A condition that the investigator determines would prevent the patient from participation.
About the study
This study is assessing the accuracy of continuous glucose monitors during surgical procedures requiring anesthesia.
Sponsor: University of Colorado, Denver · Participants: 120 · Started: Aug 21, 2024
Contact the study team
- Erin Cobry, MD · Phone: 3037242323
Official record on ClinicalTrials.gov — NCT06575842
Locations in the U.S.
| Colorado | Barbara Davis Center, Aurora |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.