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
200 participants
OBSERVATIONAL
2020-09-01
2021-01-31
Brief Summary
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Detailed Description
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Satisfaction assessment at 24 and 48 hours post operatively by self-administered survey questionnaire based on different scales: Evan-LR, Net Promotor Score, Satisfaction score.
Conditions
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Keywords
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Study Design
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OTHER
RETROSPECTIVE
Study Groups
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Qual'AXI group
patients for whom distal arm surgery was performed under Axillary Brachial Plexus Block
perioperative satisfaction assessment
Satisfaction assessment at 24 and 48 hours post operatively by self-administered survey questionnaire based on different scales: Evan-LR, Net Promotor Score, Satisfaction score.
Interventions
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perioperative satisfaction assessment
Satisfaction assessment at 24 and 48 hours post operatively by self-administered survey questionnaire based on different scales: Evan-LR, Net Promotor Score, Satisfaction score.
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* inability to fill self-administered survey questionnaire
* pregnancy and breastfeeding
* surgery \> 2 hours
* second surgical site requiring anaesthesia or analgesia
* chronic use of analgesia (including opioids) or illegal drugs
18 Years
ALL
No
Sponsors
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Centre Hospitalier Universitaire de Besancon
OTHER
Responsible Party
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Locations
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CHU de Besançon
Besançon, , France
Countries
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Central Contacts
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Facility Contacts
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Francis BERTHIER, MD
Role: primary
Other Identifiers
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P/2020/480
Identifier Type: -
Identifier Source: org_study_id