NL-OMON34710
Completed
Not Applicable
Randomised study to the efficacy and safety of Continuous Glucose Monitoring by subcutaneous measurement compared to frequent point of care measurement by Accu-Chek in critically ill patients (RESCUE) - RESCUE
Onze Lieve Vrouwe Gasthuis0 sites40 target enrollmentTBD
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- diabetes mellitus
- Sponsor
- Onze Lieve Vrouwe Gasthuis
- Enrollment
- 40
- Status
- Completed
- Last Updated
- last year
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •\-ICU patients of 18 years and older
- •\-Expected length of stay longer than 24 hours
- •\-Indication for glucose regulation with insuline. (see appendix study protocol)
Exclusion Criteria
- •\- Participation in another WMO study
- •\- No informed consent
- •\- Contra indication for the use of the AccuChek: (peritoneal dialysis, Hematocrit\< 0,20 or \> 0,65 , paracetamol intoxication)
- •\- Abdominal abnormalities that inhibit sensor insertion
- •\- Participation of the same study in an earlier ICU admittance.
Outcomes
Primary Outcomes
Not specified
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