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A comparison of arm block injection above and below the collar bone for hand surgery

Speed of Onset of Ultrasound Guided Supraclavicular and Infraclavicular Brachial Plexus Block for Ambulatory Hand Surgery

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12608000366358
Enrollment
60
Registered
2008-07-29
Start date
2008-04-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

To determine whether ultrasound guided supraclavicular block provides more rapid onset of surgical analgesia than infraclavicular block. If the primary hypothesis is confirmed, this study will provide evidence supporting the use of the supraclavicular block for hand surgery. Increased exposure of the techniques may promote their uptake in this setting.

Interventions

Infraclavicular block Infraclavicular (IB) Group The needle will be advanced just posterior to the axillary artery. Following standard intravascular injection precautions, 30mL of 2% lignocaine will then be injected. Supraclavicular(SB) Group The needle will be advanced superficially in a medial direction to just inferior to the brachial plexus cords just lateral to the subclavian artery. Following standard intravascular injection precautions, 30mL of 2% lignocaine will then be injected. The d

Infraclavicular block Infraclavicular (IB) Group The needle will be advanced just posterior to the axillary artery. Following standard intravascular injection precautions, 30mL of 2% lignocaine will then be injected. Supraclavicular(SB) Group The needle will be advanced superficially in a medial direction to just inferior to the brachial plexus cords just lateral to the subclavian artery. Following standard intravascular injection precautions, 30mL of 2% lignocaine will then be injected. The duration of each procedure is approximately 15 minutes, and the overall intervention approximately 30 minutes.

Sponsors

Dr Michael Fredrickson
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
0 to No maximum
Healthy volunteers
Yes

Inclusion criteria

Patients requiring anaesthesia for elective minor hand surgery under the care of the principal investigator

Exclusion criteria

1. Patient refusal/inability to consent 2. Allergy amide LA drugs 3. Existing neurological disorders, neuropathy of the operative extremity 4. Infection at site of needle puncture

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026