Actively Recruiting

Phase Not Applicable
Age: 18Years - 75Years
All Genders
NCT07173894

Effectiveness of Field Block Compared With Interscalene Block in Shoulder Surgery

Led by Rabin Medical Center · Updated on 2025-09-15

64

Participants Needed

1

Research Sites

74 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study will compare two different types of anesthesia used for shoulder surgery. The first method, called an interscalene block, is commonly performed by anesthesiologists and is effective for pain control but may cause side effects such as breathing problems, arm weakness, or discomfort. The second method, called a shoulder field block, is a newer technique performed by orthopedic surgeons that numbs the nerves around the shoulder without affecting breathing. Patients scheduled for shoulder surgery will be randomly assigned to receive either the interscalene block or the shoulder field block. The main goal of the study is to find out whether the shoulder field block provides pain relief that is as effective as the interscalene block, but with fewer side effects. Pain levels, patient satisfaction, length of hospital stay, need for pain medication, and any complications will be recorded and compared between the two groups. The results may help identify a safe and effective alternative anesthesia option for patients undergoing shoulder surgery.

CONDITIONS

Official Title

Effectiveness of Field Block Compared With Interscalene Block in Shoulder Surgery

Who Can Participate

Age: 18Years - 75Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 18 and 75 years
  • Scheduled for arthroscopic or open shoulder surgery
Not Eligible

You will not qualify if you...

  • Prior surgery or trauma to the shoulder
  • Revision shoulder surgery
  • Fibromyalgia
  • Pregnancy
  • Contraindications to regional anesthesia such as allergy to local anesthetics, coagulopathy, or local site infection
  • Preexisting neuropathy or myopathy of the surgical limb
  • History of chronic opioid use
  • Cognitive impairment or inability to understand pain scoring systems such as dementia

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

Rabin medical center- Hasharon hospital

Petah Tikva, Central District, Israel, 49372

Actively Recruiting

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Research Team

F

Feras Qawasmi, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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