Clinical Trials Directory

Trials / Completed

CompletedNCT04319588

Parasternal Block for Cardiac Surgery

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
126 (actual)
Sponsor
Campus Bio-Medico University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
PROCEDUREParasternal Block+ Infiltration with local anesthetic of access to thoracic drainageAfter induction of general anesthesia we will perform an ultrasound-guided Parasternal Block in association with infiltration with local anesthetic of access to thoracic drainage at the end of the intervention.
PROCEDUREInfiltration with local anesthetic of access to thoracic drainageInfiltration with local anesthetic of access to thoracic drainage at the end of the intervention.

Timeline

Start date
2020-03-06
Primary completion
2020-05-09
Completion
2020-05-19
First posted
2020-03-24
Last updated
2023-02-08

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT04319588. Inclusion in this directory is not an endorsement.