Comparative Analysis of Ultrasound-Guided Versus Landmark-Based Techniques for Regional Anesthesia in Egyptian Patients
- Conditions
- Regional Anesthesia
- Interventions
- Procedure: Patients receiving landmark-based brachial plexus blocksProcedure: Landmark-Based Brachial Plexus Block
- Registration Number
- NCT06756347
- Lead Sponsor
- Assiut University
- Brief Summary
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.
- Detailed Description
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.
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 100
-
● Adult patients aged 18-65 years undergoing upper limb surgery requiring brachial plexus block.
- Patients capable of providing informed consent
-
● 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.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Ultrasound-Guided Group Patients receiving landmark-based brachial plexus blocks Patients receiving ultrasound-guided brachial plexus blocks .o Procedure performed using a high-frequency linear ultrasound probe.Real-time visualization of the brachial plexus for precise anesthetic delivery Ultrasound-Guided Group Bupivacaine Patients receiving ultrasound-guided brachial plexus blocks .o Procedure performed using a high-frequency linear ultrasound probe.Real-time visualization of the brachial plexus for precise anesthetic delivery Landmark-Based Group Landmark-Based Brachial Plexus Block Patients receiving landmark-based brachial plexus blocks.o Procedure performed based on anatomical landmarks and palpation, without imaging assistance Landmark-Based Group Bupivacaine Patients receiving landmark-based brachial plexus blocks.o Procedure performed based on anatomical landmarks and palpation, without imaging assistance
- Primary Outcome Measures
Name Time Method Success Rate 30 minutes Proportion of patients achieving adequate anesthesia (complete sensory block) within 30 minutes of administration.
- Secondary Outcome Measures
Name Time Method
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