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Parasternal Block for Cardiac Surgery — Parasternal  

Postoperative Pain Clinical Trial

Official title:
Parasternal Block for Postoperative Analgesia in Cardiac Surgery: a Pilot Controlled Trial

Clinical Trial Summary

This study examine the effect of Parasternal Intercostal Nerve Blocks with local anesthetic on pain control in patients undergoing non-emergent cardiac surgery in a prospective controlled trial. Half of participants will receive General Anesthesia combined to parasternal block while the other half receive only General Anesthesia.

Clinical Trial Description

60 patients undergoing elective cardiac surgery will be enrolled and divided into two groups: 1. Interventional (parasternal group) 2. Case control group The "parasternal group" of patients will receive the pre-operative parasternal block (20 ml of 0.5% Ropivacaine per side) in association with infiltration with local anesthetic of access to thoracic drainage (drainage infiltration with 20 ml of 0.25% Ropivacaine) at the end of the intervention combined to General Anesthesia. The "case control group" will only receive drainage infiltration with local anesthetic and standard intraoperative management with opioids. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04319588
Study type Interventional
Source Campus Bio-Medico University
Contact
Status Completed
Phase N/A
Start date March 6, 2020
Completion date May 19, 2020
View Details
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