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Clinical Trial Summary

This is a randomized, double-blind, controlled clinical trial is to evaluate the duration of efficacy of parasternal blocks with the use of local anesthetic adjuncts for analgesia after coronary artery bypass grafting surgery.


Clinical Trial Description

This study will randomize patients to either standard pain control protocols or parasternal blocks after coronary artery bypass grafting-only surgery. This study will specifically examine the effectiveness and duration of analgesia of parasternal blocks with local anesthetic adjuncts, Dexamethasone 10mg and Dexmedetomidine 50mcg, added to the local anesthetic mixture ;


Study Design


Related Conditions & MeSH terms

  • Coronary Artery Bypass Graft Surgery

NCT number NCT05191745
Study type Interventional
Source Jewish General Hospital
Contact Matthew Cameron, Dr.
Phone 1-514-340-8222
Email [email protected]
Status Not yet recruiting
Phase Phase 3
Start date January 10, 2022
Completion date May 1, 2022

See also
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