About this trial
Regional anesthesia is a cornerstone in modern surgical practices due to its ability to provide effective pain management and reduce reliance on general anesthesia. Traditional landmark-based techniques, widely used due to their simplicity and cost-effectiveness, rely on surface anatomy and palpation to guide needle placement. However, these techniques are associated with a higher risk of complications, including failed blocks and nerve injuries.
Ultrasound-guided techniques have emerged as a safer, more precise alternative, offering real-time visualization of anatomical structures. Studies suggest that ultrasound guidance improves the success rate, reduces procedural time, and minimizes complications. Despite global advancements in ultrasound-guided regional anesthesia, limited research addresses its efficacy and safety specifically in Egyptian patients, whose unique anatomical and physiological characteristics may influence outcomes.
This study seeks to fill this knowledge gap and provide evidence-based guidance tailored to this population, focusing on brachial plexus blocks.
Eligibility criteria
Qualifiers
● Adult patients aged 18-65 years undergoing upper limb surgery requiring brachial plexus block.
Patients capable of providing informed consent
Disqualifiers
● Patients with contraindications to regional anesthesia (e.g., infection at the site, severe coagulopathy).
History of severe allergic reactions to local anesthetics.
Anatomical abnormalities affecting the brachial plexus block.
Obesity (BMI > 35) or other conditions that might confound results.
Trial design
Treatments tested in this trial
- Patients receiving landmark-based brachial plexus blocks
- Landmark-Based Brachial Plexus Block
- Bupivacaine