Comparative Study Between Two Different Approaches of Brachial Plexus Block: Supraclavicular Approach and Retroclavicular Approach
- Conditions
- Brachial Plexus Block
- Interventions
- Procedure: supraclavicular brachial plexus blockProcedure: Retroclavicular brachial plexus block
- Registration Number
- NCT05187988
- Lead Sponsor
- Sohag University
- Brief Summary
In this study investigators will compare two different approaches of brachial plexus block ;supraclavicular approach and retroclavicular approach regarding success rate, duration of block, complications
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
- 100 patients doing distal arm surgery, elective , 18 to 60 years old , will be included in double blinded randomized study.
- Patient refusal .
- local infection or deformity at the block site.
- Patient with significant neurological , psychiatric or neuromuscular disease.
- Pregnancy or lactating women .
- Coagulopathy .
- Morbid obesity .
- History of allergy to local anaesthetics
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Supraclavicular approach group supraclavicular brachial plexus block probe placed firmly over the supraclavicular fossa, parallel to the clavicle to obtain a short-axis view of the divisions of the brachial plexus and the subclavian artery, lying on the first rib After skin infiltration with lidocaine 2% a 23-gauge 70mm block needle inserted in-plane with the ultrasound beam, in a lateral-to-medial direction, until the needle tip's positioned at the junction of the first rib and subclavian artery Retroclavicular approach group Retroclavicular brachial plexus block the probe will be placed below and perpendicular to the clavicle, in a paramedian sagittal plane, medial to the coracoid process, to obtain a short-axis view of the cords of the brachial plexus and the axillary vessels. The needle will be then inserted in the supraclavicular fossa, approximately 1 cm posteriorly to the clavicle, and advanced in plane and strictly parallel to the ultrasound transducer. After passing the initial blind zone of about 2 cm caused by the acoustic shadow of the clavicle, the needle tip is constantly seen, until it is positioned posterior to the axillary artery
- Primary Outcome Measures
Name Time Method Block success rate one year Investigator will compare success rate of both types of block and which one is more likely to be successfully administrated
Duration of sensory and motor blockade one year Time which each procedure will take to block sensory and motor stimuli
Complications one year Investigators will compare complications like pneumothorax,nerve injury,bleeding and which one is more likely to cause complications
- Secondary Outcome Measures
Name Time Method Duration of procedure one year Time which took the investigator to administrate each type of block
Number of needle passes one year number of times in which needle has entered been entered into the participant in each group
Trial Locations
- Locations (1)
Sohag University Hospital
🇪🇬Sohag, Egypt