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Periarterial Injection Versus Multiple Periveural Injection

The Ultrasound Guided Periarterial Injection Technique To Axilary Brachial Plexus Block Versus Perineural Multiple InjectionTechnique

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02429141
Enrollment
50
Registered
2015-04-29
Start date
2015-01-31
Completion date
2016-06-30
Last updated
2016-08-29

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

Conditions

Contusion Wrist or Hand, Crush Injury Wrist or Hand

Brief summary

In the transarterial technique for axillary brachial plexus block, the axillary artery is intentionally punctured to indicate placement of the needle within the neurovascular sheath; local anesthetic is then injected deep and superficial to the axillary artery.

Detailed description

To lessen the risk for hematoma and intravascular injection, several modifications, such as the multi-injection perineural technique, have become popular. These techniques require a high degree of technical skill and multiple needle passes, and also carry potential for injury. In this study, the investigators will compare an ultrasound-guided equivalent of the transarterial technique (periarterial injections) to a commonly used multi-injection perineural technique.

Interventions

PROCEDUREUS-guided periarterial techique

The needle will be inserted in the axillary fossa in-plane (cranial to caudal) close to the intersection of the pectoralis and biceps muscles. Two separate injections of local anesthetic will be made deep and superficial to the axillary artery

PROCEDUREUS-guided multi-injection technique

The median, ulnar and radial nerves will be identified by ultrasound. Local anesthetic will be injected adjacent to each nerve

Sponsors

North American Institute for Continuing Medical Education (NAICE)
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

1. Inclusion criteria: \- Patients (ASA physical status I-III) scheduled to undergo hand or wrist surgery under axillary brachial plexus block 2.

Exclusion criteria

* Patients with pre-existing neuropathy * Patients with allergy to local anesthetics * Patients with prior surgery in the ipsilateral axilla * Pregnant patients * Patients with difficulties in communication

Design outcomes

Primary

MeasureTime frame
Block procedure time for the axillary brachial plexus blocktime of the block achievement will be recorded up to 15 minutes

Secondary

MeasureTime frame
Onset of the blockoutcome measure will be measured up to 30 minutes a
Time to request pain medicationparticipants will be followed for 3 days
Block success rateparticipants success or block failure within 24 hours

Countries

Belgium

Outcome results

None listed

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