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

Early Rehabilitation After Hand or Wrist Ambulatory Surgery : How to Preserve Locomotion at Home Without Rebound Pain? Study Walant Wide Awake Local Anesthesia No Tourniquet Versus Axillary Brachial Plexus Block.

Status

UNKNOWN

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT04306666

Acronym

WalantBAX

Enrollment

Registered

2020-03-13

Start date

2019-12-30

Completion date

2020-12-31

Last updated

2020-03-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hand Surgery, Wrist Surgery

Keywords

Regional anesthesia, Walant block

Brief summary

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.

Detailed 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

Interventions

OTHERRegional anesthesia

Injection of local anesthetics by a regional anesthesia named Walant block (Wide Awak Local anesthesia No Tourniquet)or by axillary brachial plexus block.

Study design

Observational model

OTHER

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Inclusion criteria

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

Exclusion criteria

\- NA

Design outcomes

Primary

Measure	Time frame	Description
duration of analgesia	24 hours	time to first rescue analgesic request (opioid)

Secondary

Measure	Time frame	Description
maximal pain score during the first 24 hours after surgery	24 hours	Pain assessments during first 24 hours : maximal pain score during the first 24 hours after surgery
total rescue analgesia amounts the first 24 hours after surgery	24 hours	Pain assessments during first 24 hours : total rescue analgesia amounts the first 24 hours after surgery
duration of sensory block	24 hours	Pain assessments during first 24 hours : duration of sensory block

Countries

France

Contacts

Primary Contactolivier CHOQUET, PhD

o-choquet@chu-montpellier.fr467338256

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026