Status:

COMPLETED

Continuous Glucose Monitoring by Subcutaneous Measurement Compared to Frequent Point of Care Measurement by Accu Chek in Critically Ill Patients

Lead Sponsor:

Onze Lieve Vrouwe Gasthuis

Conditions:

Hyperglycaemia

Hypoglycaemia

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

The purpose of this study is to evaluate the accuracy and reliability of the continuous glucose monitoring system the FreeStyle Navigator® (Abbott, Diabetes Care) in critically ill patients by compari...

Detailed Description

Most patients admitted to the ICU are treated with intensive insulin therapy, according to a locally developed glucose treatment protocol. The use of a continuous glucose monitoring in critically ill ...

Eligibility Criteria

Inclusion

  • ICU-patients \> 18 years
  • Expected length of stay on the ICU \> 24 hours
  • Indication for glucose regulation with insulin (according to the current glucose treatment protocol)
  • Availability of the Freestyle Navigator

Exclusion

  • Participation in another trial subject to the WMO
  • Lack of informed consent
  • Contraindication for the use of the Accu Chek (for example peritoneal dialysis, Ht \<0,20 of \> 0,65; paracetamol intoxication)
  • Contraindication for placement of the subcutaneous glucose sensor
  • Participation in this trial during previous ICU admittance

Key Trial Info

Start Date :

December 1 2010

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

June 1 2012

Estimated Enrollment :

178 Patients enrolled

Trial Details

Trial ID

NCT01526044

Start Date

December 1 2010

End Date

June 1 2012

Last Update

June 27 2012

Active Locations (1)

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Onze Lieve Vrouwe Gasthuis

Amsterdam, Netherlands