Description Module
The Description Module contains narrative descriptions of the clinical trial, including a brief summary and detailed description. These descriptions provide important information about the study's purpose, methodology, and key details in language accessible to both researchers and the general public.
Description Module path is as follows:
Study -> Protocol Section -> Description Module
Description Module
Ignite Creation Date:
2025-12-24 @ 4:40 PM
Ignite Modification Date:
2025-12-24 @ 4:40 PM
NCT ID:
NCT04306666
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
Study:
NCT04306666
Study Brief:
Protocol Section:
NCT04306666