Erector spinae plane block for post-operative analgesia management following video-assisted thoracoscopic surgery

Completed

• Conditions: post-opereratieve pijn; post-operative pain; 10027656

• Registration Number: NL-OMON49968
• Lead Sponsor: Sint Antonius Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 60

Inclusion Criteria

Patients undergoing wedge resection or lobectomy through VATS

Exclusion Criteria

contraindications for ESPB

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The postoperative pain assessment is performed using NRS score (0 = no pain, 10<br /><br>= most severe pain felt). Pain score at rest, while coughing and during<br /><br>mobilisation will be recorded at 0, 2, 4, 8, 12 and 24hours postoperatively and<br /><br>at day 2, two times a day at 08:00 and 20:00. Measured by a nurse who is<br /><br>trained to take NRS scores.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>• Total opioid consumption in milligrams after 24 hours and 48 hours.<br /><br>• Length of stay at the recovery unit in minutes<br /><br>• Patient satisfaction (NRS 0-10)<br /><br>• Hospital length of stay in days<br /><br>• Nausea, vomiting (yes / no) day 0 and 1 post-operatively requested in the<br /><br>evening.<br /><br>• Adverse events (pneumonia: diagnosed with a chest x-ray and positive sputum<br /><br>culture)</p><br>