Actively Recruiting

Phase Not Applicable
Age: 21Years - 65Years
All Genders
NCT06969625

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

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

60

Participants Needed

1

Research Sites

34 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Shoulder pain is frequently encountered in the medical field. Rotator cuff tears are the most common cause. Shoulder pain affects quality of life and delay rehabilitation programs. Effective control of post operative pain is a cornerstone in the success of these surgeries. Regional anaesthesia is often favoured for shoulder surgery as it could effectively provide anaesthesia and postoperative analgesia. Additionally, the upper limb has multiple nerve targets that can be blocked. Ultrasound combined SSNB-ANB were described as an alternative to interscalene nerve block for shoulder surgeries equipotent pain relief and patient satisfaction as well as fewer complications due to the location of injection. Ultrasound guided SHAC block is a motor sparing block which targets all nerves supplying shoulder consistently at two sites. It was validated in chronic shoulder pain patients. However, there is no sufficient evidence for this block in postoperative pain after shoulder surgery.

CONDITIONS

Official 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...

  • Patients acceptance
  • Age between 21 and 60 years
  • Both males and females
  • Physical status ASA 1 or II
  • Body mass index (BMI) 30 kg/m2 or less
  • Undergoing arthroscopic rotator cuff repair surgery
  • Surgery duration within 2 hours
Not Eligible

You will not qualify if you...

  • Contraindications to regional blocks such as coagulopathy or infection at injection site
  • Known allergy to study drugs
  • Neuropathy in the limb undergoing surgery
  • Advanced liver, kidney, heart, or neurologic diseases
  • History of previous shoulder operation or fracture
  • Conversion from arthroscopic to open surgery
  • Pregnant females
  • Chronic opioid use

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

Zagazig University Hospitals

Zagazig, Al Sharqia, Egypt, 44519

Actively Recruiting

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Research Team

S

Sherif M. S. Mowafy, 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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