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

Hand Surgery Clinical Trial

— WalantBAX  

Official title:

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.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04306666
• Other study ID #: RECHMPL19_0429
• Status: Recruiting
• Start date: December 30, 2019
• Est. completion date: December 31, 2020

Study information

• Verified date: March 2020
• Source: University Hospital, Montpellier
• Contact: olivier CHOQUET, PhD
• Phone: 467338256
• Email: o-choquet[@]chu-montpellier.fr
• Is FDA regulated: No
• Study type: Observational

Clinical Trial 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.

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

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 31, 2020
• Est. primary completion date: December 1, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

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

Exclusion criteria:

• NA

Related Conditions & MeSH terms

• Hand Surgery
• Wrist Surgery

Intervention

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

Locations

Country	Name	City	State
France	Uhmontpellier	Montpellier

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Montpellier

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	duration of analgesia	time to first rescue analgesic request (opioid)	24 hours
Secondary	maximal pain score during the first 24 hours after surgery	Pain assessments during first 24 hours : maximal pain score during the first 24 hours after surgery	24 hours
Secondary	total rescue analgesia amounts the first 24 hours after surgery	Pain assessments during first 24 hours : total rescue analgesia amounts the first 24 hours after surgery	24 hours
Secondary	duration of sensory block	Pain assessments during first 24 hours : duration of sensory block	24 hours