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Intelligent Needle Tip Tracking Using Ultrasound Imaging for Infraclavicular Brachial Plexus Blocks

University of Oslo (UIO) logo

University of Oslo (UIO)

Status

Completed

Conditions

Nerve Block

Treatments

Procedure: Infraclavicular brachial plexus block

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT03631914
2018/1098

Details and patient eligibility

About

In a randomized controlled crossover study design, ultrasound guided infraclavicular brachial plexus blocks will be performed with and without the aid of a needle tip tracking (NTT) system. Specialists in anaesthesiology with average experience in ultrasound guided PNB techniques will perform the blocks. 26 volunteers will be included. The primary objective is to investigate the effect of the NTT system on performance time, as a measure for improved block performance. Secondary objectives are the effects of the NTT system on dexterity, peripheral nerve block characteristics, subjective experience, and peripheral block performance.

Enrollment

26 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • ASA physical status 1 or 2
  • Volunteers that have given informed written consent

Exclusion criteria

  • BMI < 18 kg/m2
  • BMI > 35 kg/m2
  • Body weight > 95 kg
  • Volunteers that cannot cooperate during the examination
  • Volunteers that do not speak or understand Norwegian language
  • Volunteers with neurologic disease, nerve- or vascular impairment
  • Volunteers with known coagulopathy
  • Volunteers that are allergic to Lidocaine or other local anaesthetic agents
  • Medications at the investigators discretion
  • Volunteers with concomitant medical treatments interfering with PNB treatment
  • Skin disease or infection affecting the whole-body surface or within the area of examination
  • Any reason why, in the opinion of the investigators, the volunteer should not participate
  • Subject participates in a potentially confounding drug or device trial during the course of the study
  • Pregnancy and lactation period
  • Women of childbearing potential who do not use an effective and secure method for birth control

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Triple Blind

26 participants in 2 patient groups

Active needle tip tracking
Active Comparator group
Description:
A needle tip tracking system is used when performing an ultrasound guided infraclavicular brachial plexus block.
Treatment:
Procedure: Infraclavicular brachial plexus block
Inactive needle tip tracking
Other group
Description:
No needle tip tracking system is used when performing an ultrasound guided infraclavicular brachial plexus block.
Treatment:
Procedure: Infraclavicular brachial plexus block

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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