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Early Rehabilitation After Hand or Wrist Ambulatory Surgery : How to Preserve Locomotion at Home Without Rebound Pain? (WalantBAX)

University Hospital Center (CHU) logo

University Hospital Center (CHU)

Status

Unknown

Conditions

Hand Surgery
Wrist Surgery

Treatments

Other: Regional anesthesia

Study type

Observational

Funder types

Other

Identifiers

NCT04306666
RECHMPL19_0429

Details and patient eligibility

About

The purpose of this retrospective study is to compare the analgesic efficacy of Walant " Wide Awake Local Anesthesia No Tourniquet " with lidocaine and bupivacaine versus axillary brachial plexus block using mepivacaïne, both performed by anesthesiologists, after hand or wrist ambulatory surgery.

The main objective is to prove that Walant block improve pain relief at home measuring time to first analgesic request.

The secondary objectives are to compare maximal pain, consumption of supplementary analgesics, and the duratin of sensory block between groups.

Full description

data will be collected on patient records and will be compared between groups of regional anesthesia.

Data will be :

  • time to first analgesic request
  • sensory block
  • rescue analgesia during the first 24 hours after surgery
  • maximal pain score during the first 24 hours after surgery
  • patient satisfaction of managing care

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All adults patients scheduled for hand or wrist ambulatory surgery since 2016

Exclusion criteria

  • NA

Trial design

60 participants in 2 patient groups

Walant group
Description:
Walant group
Treatment:
Other: Regional anesthesia
Axillary Brachial Plexus Block
Description:
Axillary Brachial Plexus Block
Treatment:
Other: Regional anesthesia

Trial contacts and locations

1

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Central trial contact

olivier CHOQUET, PhD

Data sourced from clinicaltrials.gov

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