Hand Surgery Clinical Trial
— WalantBAXOfficial 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.
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.
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 |
Country | Name | City | State |
---|---|---|---|
France | Uhmontpellier | Montpellier |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Montpellier |
France,
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 |
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