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CompletedNCT00444171Updated Mar 7, 2007

Glucose Control by eMPC Algorithm in Peri- and Postoperative Period in Cardiac Surgery Patients

An interventional study of insulin infusion rate controled by computer algorithm and insulin infusion rate guided by in-house glucose management protocol in Cardiac Surgery Patients and Blood Glucose, sponsored by Charles University, Czech Republic. Completed at 1 site in Czechia. Per ClinicalTrials.gov, last updated 2007-03-07.

Sponsored by Charles University, Czech Republic · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Sex
All
01

Study summary

Randomized controlled trial to compare blood glucose control by the model predictive control algorithm with variable sampling rate (eMPC) with routine glucose management protocol (RMP) in peri- and postoperative period in cardiac surgery patients.

Read the detailed description

Context. Increased blood glucose levels frequently occur in critically ill patients and its normalization by intensive insulin treatment markedly improves clinical outcome.

Objective and Design: Randomized controlled trial to compare blood glucose control by the model predictive control algorithm with variable sampling rate (eMPC) with routine glucose management protocol (RMP) in peri- and postoperative period in cardiac surgery patients.

Setting: Department of Cardiac Surgery, University Hospital. Patients. 60 cardiac surgery patients. Interventions. Elective cardiac surgery and treatment with continuous insulin infusion to maintain euglycemia (target range 4.4 - 6.1 mmol/l). 30 patients were randomized for eMPC and 30 for RMP treatment. Blood glucose was measured in 1-4 hour intervals depending on request of each algorithm during surgery and post-operation period for 24 hours.

Main Outcome Measures. Mean blood glucose, percentage of time in target range. Results. Mean blood glucose was 6.15 ± 1.11 mmol/l in eMPC vs. 7.21 ± 1.08 mmol/l in RMP group (p\<0.05); percentage of time in target range was 60.4 ± 22.8% for eMPC vs. 27.5 ± 16.2% for RMP group (p\<0.05). No severe hypoglycemia (blood glucose bellow 2.9 mmol/l) was observed during the study. Average insulin infusion rate was 4.67 ± 3.34 in eMPC vs. 2.57 ± 1.66 IU/h in RMP (p\<0.05), average sampling interval was 1.46 ± 0.31 vs. 2.10 ± 0.22 hours (p\<0.05).

Conclusions. eMPC algorithm was more effective and comparably safe as compared to RMP in maintaining euglycemia in cardiac surgery patients.

02

Conditions studied

  • Cardiac Surgery Patients
  • Blood Glucose

Keywords

  • critically ill
  • insulin resistance
  • intensive insulin therapy
  • computer algorithm
03

In context

Critical Illness

1,923 studies on the registry are indexed under Critical Illness; 465 are open to participants now.

This study's enrollment of 60 is below the median of 90 across 1,003 interventional studies indexed under Critical Illness.

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Lead sponsor

Charles University, Czech Republic is the lead sponsor of 227 studies on the registry; 76 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Elective cardiac surgery

Exclusion criteria

Exclusion Criteria:

  • Allergy against insulin
  • Mental incapacity
  • Language barrier
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
60 participants

Interventions

  • Procedureinsulin infusion rate controled by computer algorithm
  • Procedureinsulin infusion rate guided by in-house glucose management protocol
06

What researchers measure

Primary outcomes

  1. Mean blood glucose

  2. percentage of time in target range

Secondary outcomes

  1. Number of hypoglycaemic episodes

07

Study locations

1 site
  • General University Hospital
    Prague, 12808, Czechia
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 7, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00444171
First posted
Mar 7, 2007
Start date
Sep 2006
Completion
Feb 2007
Last update
Mar 7, 2007

Study contacts

Stepan Svacina, MD, DSc
principal investigator · Charles University Prague

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2007. You cannot join it, but the record below documents what was studied.

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