An observational study in Hand Surgery and Wrist Surgery, sponsored by University Hospital, Montpellier. Status unknown at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-03-13.
Sponsored by University Hospital, Montpellier · Observational
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.
data will be collected on patient records and will be compared between groups of regional anesthesia.
Data will be :
University Hospital, Montpellier is the lead sponsor of 1,244 studies on the registry; 225 are open to participants now.
Counted across the registry records on this site, refreshed daily.
All adults patients scheduled for hand or wrist ambulatory surgery
Exclusion criteria:
Walant group
Other: Regional anesthesia
Axillary Brachial Plexus Block
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.
duration of analgesia
time to first rescue analgesic request (opioid)
Time frame: 24 hours
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
Time frame: 24 hours
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
Time frame: 24 hours
duration of sensory block
Pain assessments during first 24 hours : duration of sensory block
Time frame: 24 hours
Plan to share: Undecided — NC
No publications or documents are linked to this record.
This study is status unknown, as verified in Mar 2020. You cannot join it, but the record below documents what was studied.
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University Hospital, Montpellier