Accuracy of continuous glucose monitoring in cardiac surgery

Not Applicable

• Conditions: Not Applicable

• Registration Number: KCT0009396
• Lead Sponsor: The Catholic University of Korea, Seoul St. Mary's Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 27 May 2024

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 42

Inclusion Criteria

A patient or legal representative voluntarily decides to participate in this clinical study and signs and seals the subject's written consent to participate in the study

Exclusion Criteria

1. Patient scheduled for emergency surgery
2. Patient who cannot communicate
3. Patient who is pregnant or nursing
4. Patient who is unable to insert a sensor into the rear of the upper arm
5. Patients taking drugs (Hydroxyurea, acetaminophen, paracetamol) that can affect the sensor

Study & Design

• Study Type: Observational Study
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Agreement rate 20/20

Secondary Outcome Measures

Name	Time	Method
Agreement rate 15/15;Agreement rate 30/30;Agreement rate 40/40;Mean absolute relative difference;FDA continuous glucose monitoirng system validation criteria;Sensor failture rate;Adverse event rate;Patient satisfaction;Error grid analysis