Overview

Ropivacaine Though Laterosternal Catheters After Cardiac Surgery

Status:
Completed
Trial end date:
2010-11-01
Target enrollment:
Participant gender:
Summary
This is a prospective double-blinded and randomised study involving patients undergoing cardiac surgery with median sternotomy, the effects on postoperative analgesia of a 48-hr continuous infusion of ropivacaine 2 mg.mL-1, at the rate of 4 mL.hr-1 through two catheters inserted at the lateral edges of the sternum will be studied, versus a control group in which normal saline will be infused in the same conditions.
Phase:
Phase 4
Details
Lead Sponsor:
University Hospital, Clermont-Ferrand
Treatments:
Ropivacaine