Actively Recruiting
Comparison of Postoperative Analgesic Efficacy of SPSIPB and Combination of IBPB and SCPB
Led by Ankara Etlik City Hospital · Updated on 2025-03-14
80
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Shoulder arthroscopy is one of the frequently performed surgical procedures today. After shoulder surgery, ensuring sufficent analgesia is necessary for both the patient's comfort and for the early and regular performance of the required postoperative rehabilitation exercises. Nerve blocks provide better pain control, opioid consumption in the postoperative period, and consequently have advantages such as fewer side effects and lower risks of pulmonary and cardiac complications. Multimodal analgesia approach is preferred for patients undergoing shoulder arthroscopy. Along with intravenous analgesic agents, peripheral nerve blocks (applied to every suitable and consenting patient) are performed based on patient preference. This study aims to compare the analgesic efficacy in the postoperative period of patients undergoing shoulder arthroscopy with a combination of interscalene brachial plexus block and superficial cervical plexus block with serratus posterior superior intercostal plane block.
CONDITIONS
Official Title
Comparison of Postoperative Analgesic Efficacy of SPSIPB and Combination of IBPB and SCPB
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age between 18 and 65 years
- American Society of Anesthesiologists (ASA) physical status I, II, or III
- Body mass index (BMI) between 18 and 30 kg/m2
- Scheduled for elective shoulder arthroscopy surgery
You will not qualify if you...
- Under 18 or over 65 years old
- ASA score IV or higher
- Advanced co-morbid conditions
- History of bleeding diathesis
- Body mass index (BMI) under 18 kg/m2 or over 30 kg/m2
- Refusal to undergo the procedure
- Previous shoulder surgery
- Chronic use of opioids or analgesics
- Emergency shoulder surgery
- Not undergoing shoulder surgery
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Ankara Etlik City Hospital
Yenimahalle, Ankara, Turkey (Türkiye), 06170
Actively Recruiting
Research Team
M
MÜRÜVVET TAŞKIR TURAN, MD
CONTACT
M
MUSA ZENGİN, Associate Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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