Status:

COMPLETED

Efficacy of Ultrasound-guided Axillary Nerve Block Versus Ultrasound-guided Peripheral Forearm Block in Patients Undergoing Hand Surgery

Lead Sponsor:

Jessa Hospital

Conditions:

Surgery

Anesthesia, Local

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

By means of an observer-blinded, mono-center, prospective, randomized controlled superiority trial, the total anesthesia-related time (sum of performance and onset times) of an ultrasound-guided dista...

Detailed Description

Introduction: Regional anesthesia (RA) has become an increasingly popular alternative for general anesthesia in day-care hand surgery. It has been demonstrated to allow faster recovery and to reduce ...

Eligibility Criteria

Inclusion

  • ≥18 years old
  • ASA (American Society of Anesthesiology) classification: 1 - 3
  • Scheduled for surgery in the day surgery unit
  • Patients planned for unilateral hand surgery: carpal tunnel release, finger amputation (except digit I and II), finger manipulation (except digit I and II), hand foreign body removal (except digit I and II), hand incision and drainage, metacarpal fracture repair (except digit I and II), trigger finger release (except digit I), tendon repair (except digit I), and Dupuytren's contracture (except digit I)

Exclusion

  • Refusal of the patient
  • Bilateral surgery
  • BMI ≥ 40 kg/m²
  • Puncture site infections
  • Preexisting peripheral neuropathy
  • Chronic pain syndrome
  • Diabetes mellitus
  • Pregnancy
  • Use of strong pain medication in the past 3 months
  • Allergy for any of the medications used
  • Coagulation disorders or the use of anticoagulant therapy (vitamin K antagonists, new oral anticoagulants) or antiplatelet drugs (thienopyridines)
  • Contra-indication for the use of a tourniquet
  • Previous surgery in the same upper extremity
  • Impossibility to understand the study protocol
  • Not understanding the Dutch language

Key Trial Info

Start Date :

January 13 2021

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 31 2021

Estimated Enrollment :

80 Patients enrolled

Trial Details

Trial ID

NCT04678765

Start Date

January 13 2021

End Date

October 31 2021

Last Update

November 19 2021

Active Locations (1)

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Jessa Hospital

Hasselt, Limburg, Belgium