Skip to main content
OpenTrials
Completed

NCT Number: NCT03290404

Descriptive Assessment of Practice in Anaesthesia : Lidocaine 1% Adrenaline Under in Axillary Block Realization

Axillary block is the good anesthetic technique for upper limb surgery without exceeding a certain total dose injected of Local Anesthetic (AL).

The maximal recommended dose of Lidocaine adrenaline in the upper limb is 500 mg. The use of ultrasound helps guiding the locoregional anesthesia, and allows to decrease the AL concentration, thus decreasing the risks.

No previous study estimated a concentration of lidocaine lower than 1,5 % to realize upper limb surgery by axillary block.

The literature overestimating probably the rate of failure of the locoregional anesthesia under ultrasound-guidance, we suggest to estimate the rate of failure of the axillary block ultrasound-guided with the lidocaine 1 % adrenaline for realizing upper limb surgery in standard practice.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHRU de Brest, Brest, France

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients operated for the upper limb under block axillaire
  • Adult
  • non-opposition

Exclusion criteria

  • medical advice to realize axillary block
  • medical advice to local anaesthetic
  • Allergy
  • Pregnant
  • ASA 3 or more

Treatment and study plan

Primary outcomes

  1. Resort to an anesthesia for help in case of ineffectiveness of the block

    Time frame: Day 1

    Yes or no Yes or No

Secondary outcomes

  1. Block depth

    Time frame: Day 1

    Bromage score

Other outcomes

  1. Time of Block

    Time frame: Day 1

    Minutes

  2. Total dose of Lidocaïne adrenaline used

    Time frame: Day 1

    mg

  3. Patient satisfaction

    Time frame: Day 1

    questionnaire score

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Registry information

Acronym: fLACON

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Sep 21, 2017
Registry last updated
Apr 6, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.