Plexus Brachialis Block. Better to do by Start Than by End of Surgery?
NCT ID: NCT01740141
Last Updated: 2016-04-06
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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COMPLETED
NA
52 participants
INTERVENTIONAL
2012-11-30
2016-04-30
Brief Summary
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This is a prospective, randomized, double blind study in patients with radial fractures undergoing surgery with volar plate. The patients will be followed up for 6 months after surgery.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Plexus before surgery
Plexus brachialis before surgery
Plexus brachialis block
Plexus after surgery
Plexus brachialis performed after surgery
Plexus brachialis block
Interventions
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Plexus brachialis block
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* ASA 1 and 2
* Able to communicate in norwegian
* Suitable for surgery in general anaesthesia and brachial plexus block
Exclusion Criteria
* Chronic pain
* BMI over 35
18 Years
70 Years
ALL
No
Sponsors
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Oslo University Hospital
OTHER
Responsible Party
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Anne Holmberg
Principal investigator
Principal Investigators
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Anne Holmberg, MD
Role: PRINCIPAL_INVESTIGATOR
MD Ullevaal sykehus
Locations
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Oslo Universitetssykehus, Ullevaal, dept of anaesthesiology, legevakten
Oslo, Oslo County, Norway
Countries
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Other Identifiers
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2011/476a
Identifier Type: -
Identifier Source: org_study_id
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