sability of Subcutaneous Continuous Glucose Monitoring in Critically Ill Patients.
Recruiting
- Conditions
- Blood glucose monitoring, critically ill patients
- Registration Number
- NL-OMON29113
- Lead Sponsor
- Academic Medical Center
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 50
Inclusion Criteria
1. Patient is at least 18 years old;
2. Patient is admitted to the ICU of the Academic Medical Center, The Netherlands;
Exclusion Criteria
1. Patient currently has a suspected or diagnosed medical condition that, in the opinion of the Investigator, warrants exclusion from the study or prevents the patient from completing the study;
2. Patient is currently participating in another investigational drug or device study;
Study & Design
- Study Type
- Observational non invasive
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary objective of this study is to determine the accuracy of subcutaneous CGM glucose measurements as compared with current standard of care blood glucose levels measurements.
- Secondary Outcome Measures
Name Time Method The secondary objective of this study is to train healthcare workers to use of the Medtronic Sentrino® system, and to obtain feedback from the users on the usability of the Medtronic Sentrino® system.