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Clinical Trials/NL-OMON34710
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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Observational invasive

Investigators

Sponsor
Onze Lieve Vrouwe Gasthuis

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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