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Clinical Trials/CTRI/2025/08/092271
CTRI/2025/08/092271
Not yet recruiting
Phase 4

Comparison of efficacy of three different local anaesthetic mixtures for upper limb surgeries under usg guided supraclavicular brachial plexus block a randomised controlled trial

Ballari medical College and research centre1 site in 1 country78 target enrollmentStarted: August 18, 2025Last updated:

Overview

Phase
Phase 4
Status
Not yet recruiting
Sponsor
Ballari medical College and research centre
Enrollment
78
Locations
1
Primary Endpoint
Onset of sensory and motor blockade

Overview

Brief Summary

Combining local anesthetics (LAs) to achieve both rapid onset and prolonged duration has been practiced for over 50 years. While some studies have shown benefits—such as faster onset with a 40 mL mixture of mepivacaine and bupivacaine in infraclavicular blocks—others found no advantage at lower volumes (e.g., 30 mL in interscalene blocks). Advances in ultrasound-guided techniques have enabled effective brachial plexus blocks with lower volumes (10–20 mL), especially in the supraclavicular region. However, most studies focus on higher volumes. This study aims to evaluate the characteristics of a 20 mL mixture of local anesthetics for ultrasound-guided supraclavicular brachial plexus block.

Study Design

Study Type
Interventional
Allocation
Randomized
Masking
Participant and Outcome Assessor Blinded

Eligibility Criteria

Ages
18.00 Year(s) to 60.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Patients belonging to the age group 18-60 years with ASA grade I and grade II undergoing elective or emergency procedure for upper limb bone surgeries at or below the elbow.

Exclusion Criteria

  • Patient refusal for the block.
  • Patients refusing the block will be administered general anaesthesia.
  • History of bleeding disorders Local infection at the site of block Pre-existing neurological deficit Cardio-Respiratory compromise.
  • Known allergy to local anesthetic drug.
  • Patients in whom the supraclavicular sonoanatomy is not clear.

Outcomes

Primary Outcomes

Onset of sensory and motor blockade

Time Frame: 0,5,10,15,20,25,30,35,40minutes

Secondary Outcomes

  • Duration of analgesia and anaesthesia(0,5,10,15,20,25,30,35,40minutes)

Investigators

Sponsor
Ballari medical College and research centre
Sponsor Class
Government medical college
Responsible Party
Principal Investigator
Principal Investigator

AJJAYYA ABBIGERI HIREMAT

Department of ANAESTHESIOLOGY

Study Sites (1)

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