Actively Recruiting
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
Eligibility Criteria
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.
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
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)
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
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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