ClinicalTrials.gg
CompletedNCT02429141Updated Aug 29, 2016

Periarterial Injection Versus Multiple Periveural Injection

An interventional study of US-guided periarterial techique and US-guided multi-injection technique in Contusion Wrist or Hand and Crush Injury Wrist or Hand, sponsored by North American Institute for Continuing Medical Education (NAICE). Completed at 1 site in Belgium. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2016-08-29.

Sponsored by North American Institute for Continuing Medical Education (NAICE) · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
50
Allocation
Randomized
Ages
18 Years to 90 Years
Sex
All
01

Study 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.

Read the 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.

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Conditions studied

  • Contusion Wrist or Hand
  • Crush Injury Wrist or Hand
03

In context

Contusions

43 studies on the registry are indexed under Contusions; 8 are open to participants now.

This study's enrollment of 50 is below the median of 90 across 31 interventional studies indexed under Contusions.

Browse Contusions studies →

Lead sponsor

North American Institute for Continuing Medical Education (NAICE) is the lead sponsor of 2 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients ( I-III) scheduled to undergo hand or wrist surgery under axillary brachial plexus block

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
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

ASA physical status

The anaesthetists’ scale of health before surgery: I is healthy, II has a mild illness that is under control, III a severe one, IV a severe illness that is a constant threat to life. V and VI are used for the critically ill and for organ donors.

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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
50 participants (actual)

Study arms

  • Experimental
    US-guided periarterial techique

    Axillary brachial plexus block by an ultrasound-guided periarterial technique

    Procedure: US-guided periarterial techique

  • Experimental
    US-guided multi-injection technique

    Ultrasound-guided multi-injection perineural technique for axillary brachial plexus

    Procedure: US-guided multi-injection 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

06

What researchers measure

Primary outcomes

  1. Block procedure time for the axillary brachial plexus block

    Time frame: time of the block achievement will be recorded up to 15 minutes

Secondary outcomes

  1. Onset of the block

    Time frame: outcome measure will be measured up to 30 minutes a

  2. Time to request pain medication

    Time frame: participants will be followed for 3 days

  3. Block success rate

    Time frame: participants success or block failure within 24 hours

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Study locations

1 site
  • Department of Anesthesiology Ziekenhuis Oost-Limburg
    Genk, Belgium
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 29, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02429141
Lead sponsor
North American Institute for Continuing Medical Education (NAICE)
Responsible party
Catherine Vanderpitt, MD (Catherine Vanderpitte, MD, North American Institute for Continuing Medical Education (NAICE)) — Principal investigator
First posted
Apr 29, 2015
Start date
Jan 2015
Primary completion
Jan 2016
Completion
Jun 2016
Last update
Aug 29, 2016

Study contacts

Admir Hadzic, MD
study director · Director

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2016. You cannot join it, but the record below documents what was studied.

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