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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.


Clinical Trial 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 ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04306666
Study type Observational
Source University Hospital, Montpellier
Contact olivier CHOQUET, PhD
Phone 467338256
Email o-choquet@chu-montpellier.fr
Status Recruiting
Phase
Start date December 30, 2019
Completion date December 31, 2020

See also
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Terminated NCT00827658 - Ulnar Nerve Block for Procedural Anesthesia - Wrist Versus Palm N/A
Completed NCT04189198 - A Comparison of 4% Articaine Versus 0.5%Bupivacaine for Ambulatory Surgery Under Supraclavicular Block Phase 1
Completed NCT00699244 - Comparison of Central Versus Peripheral Placement of Local Anesthetic N/A
Active, not recruiting NCT02073383 - Three Techniques for Ultrasound Guided Axillary Brachial Plexus Block N/A
Completed NCT03632304 - Local Anesthesia With Minimal Sedation and Brachial Plexus Block in Hand Surgery N/A
Completed NCT05325372 - A Comparative Study Between Infraclavicular and Axillary Blocks for Assessment of Motor Power Using Handgrip Dynamometer N/A