A randomized controlled trial comparing intermittent erector spinae plane block versus single shot intercostal block (SSIB) in video-assisted thoracoscopic surgery (VATS) of wedge resection and lobectomies

Withdrawn

• Conditions: surgery of lung tumours; 10029107

• Registration Number: NL-OMON46023
• Lead Sponsor: Academisch Medisch Centrum

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Withdrawn
• Sex: Not specified
• Target Recruitment: 77

Inclusion Criteria

Adult patient older than 18 years undergoing elective unilateral VATS for wedge resection, lobectomy, biopsy, resection of a nodule, or bullectomy. Patients must be able and willing to provide written informed consent.

Exclusion Criteria

Participation in another trial focusing on postoperative recovery
- Allergy to local anesthetics or morphine
- Refusal of one of the methods of analgesia
- Insufficient comprehension of the Dutch QoR-40 questionaire.
- Chronic pain, or opioid use longer than 3 months

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>QoR-40 score at day 2.</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>QoR-40 at day 1 and 3, postoperative morphine-equivalent consumption per day<br /><br>until discharge, postoperative NRS (Numeric Rating Scale) score day 1-3 (mean<br /><br>and maximum per day), postoperative VAS score (Visual Analog Scale, mean and<br /><br>maximum per day) day 1-3, LOS (Length of hospital stay), requirement of rescue<br /><br>medication, sensory block spread immediately postoperatively and on POD 1 and<br /><br>2, side effects unrelated to surgery, surgical site infection, postoperative<br /><br>pneumonia, LA toxicity (epileptic seizures). </p><br>