Interscalene Brachial Plexus Block Versus Serratus Posterior Superior Intercostal Plane Block for Arthroscopic Shoulder Surgery

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorFerit Yetik

About this trial

Arthroscopic shoulder surgery is associated with moderate to severe postoperative pain that may delay recovery and rehabilitation. Interscalene brachial plexus block (ISB) is widely used for postoperative analgesia in shoulder surgery; however, it may be associated with complications such as phrenic nerve paralysis. The serratus posterior superior intercostal plane (SPSIP) block is a recently described fascial plane block that may provide effective analgesia while avoiding some of the limitations of ISB.

This prospective, randomized, double-blind controlled trial aims to compare the analgesic efficacy of ISB and SPSIP block in patients undergoing elective arthroscopic shoulder surgery under general anesthesia. The primary outcome is total postoperative opioid consumption during the first 24 hours after surgery. Secondary outcomes include postoperative pain scores, quality of recovery, time to first rescue analgesia, rescue analgesic requirements, intraoperative opioid consumption, sensory block distribution, motor block characteristics, and block-related complications.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age between 18 and 75 years

ASA physical status I, II, or III

Scheduled for elective arthroscopic shoulder surgery under general anesthesia

Provision of written informed consent

Disqualifiers

Refusal to participate in the study

Coagulopathy

Current anticoagulant therapy

Infection at the block site

Trial design

Design model

Parallel

Treatments tested in this trial

  • Interscalene Brachial Plexus Block

    Procedure/Surgery

    Ultrasound-guided interscalene brachial plexus block performed before induction of general anesthesia for postoperative analgesia in arthroscopic shoulder surgery.

  • Serratus Posterior Superior Intercostal Plane Block

    Procedure/Surgery

    Ultrasound-guided serratus posterior superior intercostal plane block performed before induction of general anesthesia for postoperative analgesia in arthroscopic shoulder surgery.

  • Bupivacaine

    Drug

    Bupivacaine administered for ultrasound-guided regional anesthesia block.

Treatment groups

80 Participants
are divided into 2 treatment groups
Group A: Interscalene Brachial Plexus Block GroupExperimental treatment 2 interventions
Group B: Serratus Posterior Superior Intercostal Plane Block GroupExperimental treatment 2 interventions

Trial outcomes

Primary outcomes

1

Total Opioid Consumption During the First 24 Postoperative Hours

Comparison of total postoperative opioid consumption between the interscalene brachial plexus block group and the serratus posterior superior intercostal plane block group during the first 24 hours after surgery.

Time frame
24 hours after surgery

Secondary outcomes

1

Postoperative Pain Scores

Numeric Rating Scale (NRS) pain scores at rest and during movement, ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain.

Time frame
0, 2, 4, 8, 16, and 24 hours after surgery
2

Quality of Recovery (QoR-15)

Quality of Recovery-15 (QoR-15) score assessed 24 hours after surgery. Scores range from 0 to 150, with higher scores indicating better postoperative recovery and patient satisfaction.

Time frame
24 hours after surgery
3

Intraoperative Remifentanil Consumption

Total remifentanil consumption during surgery.

Time frame
During surgery
4

Time to First Rescue Analgesic Requirement

Time elapsed from the end of surgery to the first rescue analgesic administration.

Time frame
First 24 postoperative hours

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Ferit Yetik

Lead sponsor

Bursa Yuksek Ihtisas Training and Research Hospital

Sponsor institution

Bursa Sehir Hastanesi

Collaborator