Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT07278050

Interscalene Block vs Serratus Posterior Superior Intercostal Plane Block

Led by Medipol University · Updated on 2026-01-14

60

Participants Needed

1

Research Sites

41 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Postoperative pain is important following arthroscopic shoulder surgery. Postoperative effective pain treatment provides early mobilization and a shorter hospital stay. Ultrasound (US)-guided brachial plexus blocks, such as interscalene and supraclavicular block, are usually performed. Interscalen brachial plexus block (ISCB) is one of the most preferred techniques among these. Ultrasound (US) guided serratus posterior superior block (SPSPB) is a new interfacial plane block defined by Tulgar et al in 2023. It is based on injection on the serratus posterior superior muscle at the level of the 2nd or 3rd rib. This block provides analgesia in conditions such as interscapular pain, chronic myofascial pain syndromes, scapulocostal syndrome, and shoulder pain. The SPS muscle is located at the C7-T2 level. It attaches to the lateral edges of the second and fifth ribs. It is innervated by the lower cervical and upper intercostal nerves. With the SPS block, these nerves are blocked, and analgesia is provided. It has been reported that SPSIPB provides effective analgesia after shoulder surgery. The aim of this study is to compare the efficacy of the US-guided SPSIPB and ISCB for postoperative analgesia management after arthroscopic shoulder surgery.

CONDITIONS

Official Title

Interscalene Block vs Serratus Posterior Superior Intercostal Plane Block

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • American Society of Anesthesiologists (ASA) classification I-II
  • Scheduled for arthroscopic shoulder surgery under general anesthesia
Not Eligible

You will not qualify if you...

  • History of bleeding diathesis
  • Receiving anticoagulant treatment
  • Known allergy to local anesthetics or opioids
  • Infection of the skin at the needle puncture site
  • Pregnancy or lactation
  • Patients who do not accept the procedure

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Istanbul Medipol University Hospital

Istanbul, Bagcilar, Turkey (Türkiye), 34070

Actively Recruiting

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Research Team

B

Bahadir Ciftci, Assoc Prof, MD

CONTACT

Y

Yunus Atalay, Prof, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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