Axillary Plexus Block in a High Resolution MRI

NCT01033006 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 45

Last updated 2014-02-13

No results posted yet for this study

Summary

Background and aims:

Magnetic resonance imaging (MRI) has proved beneficial for presenting anatomy for regional anaesthesia and to demonstrate spread of local anaesthetic.

A new axillary plexus block with a triple injection (1), combining a short axillary catheter method with a transarterial axillary block, is now being evaluated with a 3 Tesla MRI. In this study, the investigators are investigating MR visualisation of three different block techniques and compare the clinical efficacy of the techniques, with the MR findings.

Patients \& Methods:

After obtaining approval of the protocol from the regional ethical committee, 3 x 15 adult patients, scheduled for hand surgery, were included in a randomised, blinded prospective study.

Conditions

  • Nerve Block
  • Magnetic Resonance Imaging

Interventions

PROCEDURE

Active Comparator: Arm 1: catheter injection

PROCEDURE

Active Comparator: Arm 2: transarterial injection

PROCEDURE

Active Comparator: Arm 3: catheter and transarterial injection

Sponsors & Collaborators

  • Oslo University Hospital

    collaborator OTHER
  • Diakonhjemmet Hospital

    lead OTHER

Principal Investigators

  • Trygve TK Kjelstrup, MD · Diakonhjemmet Sykehus, University of Oslo

  • Øivind ØK Klaastad, PhD, MD · Rikshospitalet, Dep. of Anesthesiology, Oslo University Hospital

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-01-31
Primary Completion
2011-02-28
Completion
2012-08-31

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01033006 on ClinicalTrials.gov