Accuracy of Continuous Glucose Monitors During the Perioperative Period in Youth With Type 1 Diabetes
Recruiting now
Conditions studied: Type 1 Diabetes
In brief
This study is assessing the accuracy of continuous glucose monitors during surgical procedures requiring anesthesia.
Key facts
- Study ID
- NCT06575842
- Run by
- University of Colorado, Denver
- People needed
- 120
- Starts
- 2024-08-21
- Expected to finish
- 2027-12-01
- Last updated by the study team
- 2026-06-12
Who can join
Age: 2 and older, up to 26. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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.
You may not qualify if…
- Pregnancy.
- Currently using hydroxyurea.
- A condition that the investigator determines would prevent the patient from participation.
Where it is running
- Barbara Davis Center — Aurora, Colorado, United States (enrolling)
Full record on ClinicalTrials.gov
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