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Ultrasound-Guided Axillary or Infraclavicular Nerve Block for Upper Limb Surgery

Onset Time of Brachial Plexus Anesthesia With the Axillary or Infraclavicular Approach Under Real-Time Ultrasound Guidance: a Randomized Controlled Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00724035
Enrollment
52
Registered
2008-07-29
Start date
2008-05-31
Completion date
2009-07-31
Last updated
2009-07-15

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

Conditions

Forearm Injuries, Nerve Block, Orthopedic Surgery, Trauma, Upper Extremity

Keywords

Anesthesia, Upper extremity, Nerve block, Ultrasound, Brachial plexus

Brief summary

This study aims to detect differences in onset time of brachial plexus (i.e., arm) anesthesia using two different nerve block techniques. Using ultrasound guidance, axillary (i.e., at the armpit) and infraclavicular (i.e., below the collarbone) blocks will be performed to patients undergoing upper limb surgery. The investigators will analyze how long it takes for anesthesia to be adequate for pain-free surgery, thus determine the optimal technique for this kind of surgery.

Detailed description

Real-time ultrasound guidance has substantially reduced the risk of pneumothorax and/or vascular puncture during infraclavicular brachial plexus blocks. The role of this technique has thus been expanded to overlap those procedures for which an axillary nerve block would be commonly considered as first choice. A reference block for upper limb surgery thanks to its safety profile and clinical efficacy, the axillary approach may be more painful or unpleasant for some patients. The investigators aim to determine possible differences in onset time and patient acceptance between the two techniques.

Interventions

DRUGMidazolam

Procedural sedation before the execution of the block. * 0.03 mg/kg iv bolus

DRUGRopivacaine

0.75% (wt/vol) solution, 20 ml perineural injection

DRUGFentanyl

50 µg iv bolus prn for pain during surgery, up to 150 µg

PROCEDUREGeneral anesthesia

General anesthesia will be induced if pain during surgery develops which is intractable with iv fentanyl ≤150 µg.

PROCEDUREAxillary brachial plexus nerve block

Blocks will be performed under high-resolution real-time ultrasound guidance. Patients will be in the supine position. With the abducted arm flexed 90° at the elbow, the transducer will scan for the axillary artery in its short-axis. Individual nerves will be sought for around the artery. A 22G, 17°-bevel needle will be advanced in-plane to inject aliquots of local anesthetic around each nerve structure up to the prescribed dose.

Blocks will be performed under high-resolution real-time ultrasound guidance. Patients will be in the supine position. The linear transducer will be initially positioned between the middle and lateral third of the clavicle, scanning on a parasagittal plane. The axillary artery and veins will then be sought for. We will try to visualize the three cords of the brachial plexus separately, and to inject local anesthetic around each of them. If this is not possible, the needle will be positioned cranially and posteriorly to the artery, and the injection will be made from there. A 20 G, 17°-bevel needle will be used for all blocks.

Sponsors

University of Parma
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* ASA Physical Status Class \<4 * Scheduled upper extremity orthopedic surgery

Exclusion criteria

* Psychiatric or cognitive disorder * Allergy to study drugs * Contraindication to nerve block at the assigned site

Design outcomes

Primary

MeasureTime frame
Onset time of brachial plexus sensory blockq5min up to 30 min after the block

Secondary

MeasureTime frame
Onset of brachial plexus motor blockq5min up to 30 min after the block
Patient satisfaction (3-point scale)End of surgery
Anesthesia-related procedural pain (0-10 numerical rating scale)End of block placement
Rescue analgesic requirements during surgeryDuring surgery

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026