Early Rehabilitation After Hand or Wrist Ambulatory Surgery : How to Preserve Locomotion at Home Without Rebound Pain?
NCT ID: NCT04306666
Last Updated: 2020-03-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
60 participants
OBSERVATIONAL
2019-12-30
2020-12-31
Brief Summary
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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.
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Detailed Description
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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
Conditions
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Study Design
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OTHER
RETROSPECTIVE
Study Groups
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Walant group
Walant group
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.
Axillary Brachial Plexus Block
Axillary Brachial Plexus Block
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.
Interventions
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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.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
18 Years
ALL
No
Sponsors
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University Hospital, Montpellier
OTHER
Responsible Party
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Principal Investigators
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olivier CHOQUET, PhD
Role: STUDY_DIRECTOR
University Hospital, Montpellier
Locations
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Uhmontpellier
Montpellier, , France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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RECHMPL19_0429
Identifier Type: -
Identifier Source: org_study_id
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