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Clinical Trial Summary

A randomized, controlled trial evaluating the effect of the administration of a Maltodextrin solution in type 2 diabetic patients undergoing cardiac surgery.


Clinical Trial Description

This is a randomized, controlled, feasibility trial. The primary objective is to evaluate the feasibility of having patients receive the preoperative drink within 2 to 3 hours before induction of anesthesia and consume the entire solution within the suggested 15 minutes. The secondary objective is to compare insulin sensitivity in type 2 diabetic cardiac surgery patients who received maltodextrin before surgery versus type 2 diabetic patients who have only received water. The hyperinsulinemic-euglycemic insulin clamp will be performed just after the induction of anesthesia to measure insulin sensitivity. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05188222
Study type Interventional
Source Jewish General Hospital
Contact Matthew Cameron, MDCM, MPH
Phone 514-340-8222
Email [email protected]
Status Not yet recruiting
Phase Phase 4
Start date January 24, 2022
Completion date June 1, 2022

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