Comparison Between Ultrasound-Guided Costoclavicular and Lateral-Sagittal Infraclavicular Brachial Plexus Blocks in Adult Distal Upper Limb Surgeries

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age21-65
SponsorAin Shams University

About this trial

The aim of the study is to compare the onset time of the costoclavicular approach of brachial plexus block with that of the lateral-sagittal infraclavicular approach in adults distal upper limb surgeries.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

ASA physical status I-III

Distal upper limb surgery requiring brachial plexus block.

Patient approval after written and informed consent to participate.

Disqualifiers

Patient refusal.

Allergy to drugs used.

Infection at puncture site.

Coagulopathy or anticoagulant therapy.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Costoclavicular brachial plexus block

    Procedure/Surgery

    Ultrasound-guided costoclavicular brachial plexus block performed using a high-frequency linear probe. A mixture of 2% lidocaine and 0.5% bupivacaine (1:1 ratio) with a total volume of 0.3 mL/kg is injected in the costoclavicular space around the cords of the brachial plexus under real-time ultrasound guidance.

  • Lateral-sagittal infraclavicular brachial plexus block

    Procedure/Surgery

    Ultrasound-guided lateral-sagittal infraclavicular brachial plexus block performed using a high-frequency linear probe. A mixture of 2% lidocaine and 0.5% bupivacaine (1:1 ratio) with a total volume of 0.3 mL/kg is injected around the cords of the brachial plexus under real-time ultrasound guidance.

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: Lateral-sagittal infraclavicular block (LS-ICB) groupActive comparator 1 intervention
Group B: Costoclavicular block brachial plexus (CC) groupActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Time to onset of complete sensory and motor block

Time from completion of local anesthetic injection to achievement of complete sensory and motor blockade. Sensory block will be assessed using pinprick testing in the distributions of the median, ulnar, radial, and musculocutaneous nerves. Motor block will be graded using a standardized motor scale. And time will be in minutes and seconds.

Time frame
From completion of injection up to 30 minutes after block performance

Secondary outcomes

Other outcomes

Sponsors and contacts

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