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Ropivacaine After Sternotomy — NAROSYD  

Postoperative Pain Clinical Trial

Official title:
Ropivacaine Infusion to Alleviate Postoperative Pain After Cardiac Surgery

Clinical Trial Summary

Continuous ropivacaine infusion to sternotomy wound after coronary artery bypass grafting (CABG) or heart valve surgery to diminish postoperative pain.

Clinical Trial Description

A multiporous catheter will be introduced into sternotomy wound to CABG or heart valve surgery patients and continuous ropivacaine infusion 4 ml/h will be started immediately after surgery. Ropivacaine infusion will be administered during 48 postoperative hours. All patients receive patient controlled analgesia (PCA) oxycodone after extubation in the PACU. All patients receive a standardized anesthesia during surgery. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02449486
Study type Interventional
Source Kuopio University Hospital
Contact
Status Completed
Phase Phase 4
Start date January 2014
Completion date December 2017
View Details
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