Actively Recruiting

Phase Not Applicable
Age: 21Years - 65Years
All Genders
ID07090733

The Effect of Ultrasound Guided Interscalene, Suprascapular and Anterior Glenoid Nerve Blocks on Diaphragmatic Excursion and Analgesia Following Arthroscopic Shoulder Surgery: A Prospective Randomized Controlled Study

Led by Tanta University · Updated on 2025-07-29

80

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are evaluating the effects of different nerve blocks on diaphragmatic movement and pain relief after arthroscopic shoulder surgery. The study focuses on comparing anterior glenoid, suprascapular, and interscalene nerve blocks to understand their impact on postoperative pain and diaphragm function. Arthroscopic shoulder surgery often causes moderate to severe pain, especially within 48 hours post-operation, which can delay recovery. The suprascapular nerve provides about 70% of the sensory nerve fibers to the shoulder joint, making it a key target for pain control. Participants will receive general anesthesia along with one of four ultrasound-guided nerve block treatments. These include an interscalene brachial plexus block with 15 mL of 0.25% bupivacaine, a suprascapular nerve block with the same dosage, an anterior glenoid block with 15 mL of 0.25% bupivacaine, or a combination of suprascapular and anterior glenoid blocks totaling 30 mL of 0.25% bupivacaine split evenly between the two. Each treatment group is randomized and double-blinded. During the study, participants will be monitored for diaphragmatic paralysis 24 hours after surgery, which is the primary outcome. Secondary outcomes include the level of pain, total pain medication use, and patient satisfaction within the first 24 hours postoperatively. The study involves assessments to evaluate these measures following the nerve blocks and surgery. Overall, participation requires adherence to the study schedule and follow-up evaluations up to 24 hours after the procedure.

CONDITIONS

Brief Title

Ultrasound Guided Interscalene, Suprascapular and Anterior Glenoid Nerve Blocks on Diaphragmatic Excursion and Analgesia Following Arthroscopic Shoulder Surgery

Who Can Participate

Age: 21Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age from 21 to 65 years.
  • Both sexes.
  • American Society of Anesthesiologists (ASA) physical status I or II.
  • Scheduled for arthroscopic shoulder surgery.
Not Eligible

You will not qualify if you...

  • Patient's refusal to participate.
  • History of allergy to local anesthetics.
  • History of chronic use of painkillers.
  • Presence of mental dysfunction.
  • Coagulation disorders.
  • Skin or soft tissue infection at the proposed needle insertion site.
  • Pregnant patients.
  • Chronic Obstructive Pulmonary Disease (COPD) or Body Mass Index (BMI) over 40.

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.

Surgery and Immediate Post-operative Care

Duration - Day of surgery

Participants undergo arthroscopic shoulder surgery with general anesthesia and receive one of the ultrasound-guided nerve blocks for pain management.

1 visit (in-person)

Post-operative Follow-up

Duration - 24 hours postoperatively

Participants are assessed for diaphragmatic function, pain levels, analgesic use, and satisfaction after surgery.

1 follow-up visit (in-person)

Trial Site Locations

Total: 1 location

1

Tanta University

Tanta, El-Gharbia, Egypt, 31527

Actively Recruiting

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Research Team

F

Fatma E Elsamahy, Master

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

4

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