Actively Recruiting

Phase Not Applicable
Age: 21Years - 65Years
All Genders
ID06969625

Shoulder Anterior Capsular Block Versus Combined Suprascapular and Axillary Nerve Blocks for Postoperative Pain Relief in Arthroscopic Rotator Cuff Repair Surgery

Led by Zagazig University · Updated on 2025-05-14

60

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Shoulder pain often results from rotator cuff tears and can significantly affect quality of life and delay rehabilitation. This research compares two types of regional anaesthesia blocks to manage postoperative pain after arthroscopic rotator cuff repair surgery. The study aims to evaluate the analgesic effect of a newer ultrasound-guided shoulder anterior capsular block (SHAC) against the combined suprascapular and axillary nerve blocks (SSNB-ANB), which are commonly used and known for effective pain relief but with some drawbacks like motor block and diaphragm issues. The SHAC block targets all nerves supplying the shoulder consistently at two sites, aiming to spare motor function and allow early movement and rehabilitation. The SSNB-ANB block involves separate nerve blocks for the suprascapular and axillary nerves using ultrasound guidance. Both blocks use injections of bupivacaine with dexamethasone as an adjuvant. The study will randomly assign participants to receive either the SHAC block or the combined SSNB-ANB block during arthroscopic rotator cuff repair surgery. Participants will be monitored for postoperative pain using the Numeric Rating Scale at rest and movement at several intervals up to 24 hours after surgery. Researchers will measure total pethidine use in the first 24 hours, time to first request for rescue analgesia, block performance time, patient satisfaction, and any complications over seven days. The study will assess the potential benefits of the SHAC block for adequate pain control and early rehabilitation after shoulder surgery, with follow-up during the first day and up to a week after surgery.

CONDITIONS

Brief Title

Shoulder Anterior Capsular Block for Postoperative Analgesia in Arthroscopic Rotator Cuff Repair Surgery

Who Can Participate

Age: 21Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patient agrees to participate
  • Age between 21 and 60 years
  • Male or female sex
  • Physical status ASA 1 or II
  • Body mass index (BMI) of 30 kg/m2 or less
  • Scheduled for arthroscopic rotator cuff repair surgery
  • Surgery duration expected within 2 hours
Not Eligible

You will not qualify if you...

  • Contraindications to regional blocks such as coagulopathy or local infection at injection site
  • Known allergy to study drugs
  • Neuropathy affecting the limb undergoing surgery
  • Advanced liver, kidney, heart, or neurological diseases
  • History of previous shoulder surgery or fracture
  • Conversion to open surgery from arthroscopy
  • Pregnancy
  • Chronic opioid use

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - Single day of surgery and immediate postoperative period

Participants receive one of two types of nerve blocks to manage pain during and after arthroscopic rotator cuff repair surgery.

1 visit on the day of surgery

Follow-up

Duration - Up to 7 days after surgery

Participants are monitored for pain relief, analgesic use, satisfaction, and any complications following surgery.

Follow-up assessments within 24 hours and at 7 days post-surgery

Trial Site Locations

Total: 1 location

1

Zagazig University Hospitals

Zagazig, Al Sharqia, Egypt, 44519

Actively Recruiting

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Research Team

S

Sherif M. S. Mowafy, MD

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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Published Research Related To This Trial

Evaluation of Interfascial Plane and Pericapsular Nerve Blocks to the Shoulder Joint: A Preliminary Analysis of Shoulder Anterior Capsular Block.

Felice Galluccio, Mario Fajardo Perez, Ece Yamak Altinpulluk...

https://pubmed.ncbi.nlm.nih.gov/34669181

Re: "Ultrasound-Guided Block of the Axillary Nerve: A Prospective, Randomized, Single-Blind Study Comparing Interfascial and Perivascular Injections".

Felica Galluccio, Emilio Gonzalez Arnay, Carlos Salazar...

https://pubmed.ncbi.nlm.nih.gov/32013290

Efficacy and safety of suprascapular nerve block combined with axillary nerve block for arthroscopic shoulder surgery: A systematic review and meta-analysis of randomized controlled trials.

Jinlong Zhao, Nanjun Xu, Jiahui Li...

https://pubmed.ncbi.nlm.nih.gov/34520842

Comparison of Ultrasound-Guided Supra-scapular Plus Axillary Nerve Block with Interscalene Block for Postoperative Pain Management in Arthroscopic Shoulder Surgery; A Double-Blinded Randomized Open-Label Clinical Trial.

Seyed Hamid Reza Faiz, Masood Mohseni, Farnad Imani...

https://pubmed.ncbi.nlm.nih.gov/34336619

Interscalenic versus suprascapular nerve block: can the type of block influence short- and long-term outcomes? An observational study.

Michele Divella, Luigi Vetrugno, Daniele Orso...

https://pubmed.ncbi.nlm.nih.gov/29991222

Randomized, controlled trial comparing respiratory and analgesic effects of interscalene, anterior suprascapular, and posterior suprascapular nerve blocks for arthroscopic shoulder surgery.

Yean Chin Lim, Zhao Kun Koo, Vivian W Ho...

https://pubmed.ncbi.nlm.nih.gov/32668833

A randomised controlled trial of shoulder block vs. interscalene brachial plexus block for ventilatory function after shoulder arthroscopy.

P Rhyner, K Kirkham, C Hirotsu...

https://pubmed.ncbi.nlm.nih.gov/31854463