Recruiting NCT07385170
Perioperative Continuous Glucose Monitoring Accuracy in Cardiac Surgery
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Dexcom G7.
- Who it may be relevant to
- Registry conditions: Cardiac Surgery. Basic parameters: from 19 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- South Korea
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Evaluation of Perioperative Continuous Glucose Monitoring Accuracy in Patients Undergoing Cardiac Surgery
Overview
The goal of this clinical trial is to evaluate accuracy of continuous glucose monitoring device called 'Dexcom G7' in patients undergoing cardiac surgery.
Interventions
- Device Dexcom G7
Continuous glucose monitoring device (Dexcom G7) will be applied to patients undergoing cardiac surgery intraoperatively and postoperatively (maximum 10 days)
Primary outcome measures
- MARD [Time frame: From the beginning of operation to the end of postoperative ICU stay (maximum 10 days)]
Secondary outcome measures (3)
- Bland-Altman analysis [Time frame: From the beginning of operation to the end of postoperative ICU stay (maximum 10 days)]
- ISO criteria [Time frame: From the beginning of operation to the end of postoperative ICU stay (maximum 10 days)]
- DTS error grid [Time frame: From the beginning of operation to the end of postoperative ICU stay (maximum 10 days)]
Eligibility criteria
Inclusion criteria
- Patients aged 19 years or older scheduled for cardiac surgery
Exclusion criteria
- Skin disease at the sensor application site (proximal arm)
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
South Korea · 1 center
- Seoul National University Hospital — Seoul
Identifiers
NCT: NCT07385170 · CGM-CS