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Comparative Analysis of Ultrasound-Guided Versus Landmark-Based Techniques for Regional Anesthesia in Egyptian Patients

Not Applicable
Not yet recruiting
Conditions
Regional Anesthesia
Interventions
Procedure: Patients receiving landmark-based brachial plexus blocks
Procedure: 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
Inclusion Criteria
  • ● Adult patients aged 18-65 years undergoing upper limb surgery requiring brachial plexus block.

    • Patients capable of providing informed consent
Exclusion Criteria
  • ● 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
GroupInterventionDescription
Ultrasound-Guided GroupPatients receiving landmark-based brachial plexus blocksPatients 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 GroupBupivacainePatients 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 GroupLandmark-Based Brachial Plexus BlockPatients receiving landmark-based brachial plexus blocks.o Procedure performed based on anatomical landmarks and palpation, without imaging assistance
Landmark-Based GroupBupivacainePatients receiving landmark-based brachial plexus blocks.o Procedure performed based on anatomical landmarks and palpation, without imaging assistance
Primary Outcome Measures
NameTimeMethod
Success Rate30 minutes

Proportion of patients achieving adequate anesthesia (complete sensory block) within 30 minutes of administration.

Secondary Outcome Measures
NameTimeMethod
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