Dexamethasone and Analgesic Duration After Supraclavicular Brachial Plexus Blockade
NCT ID: NCT00802009
Last Updated: 2010-01-26
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
44 participants
INTERVENTIONAL
2009-05-31
2009-11-30
Brief Summary
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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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1
Dexamethasone 8mg added to routine local anesthetic during brachial plexus blockade.
Dexamethasone
Dexamethasone 8 milligrams (liquid) will be added to standard anesthetic solution administered during routine brachial plexus nerve blockade.
Mepivicaine
Standard anesthetic solution administered during routine brachial plexus nerve blockade.
2
Routine anesthetic solution (30 cc 1.5% mepivicaine) used during brachial plexus blockade.
Mepivicaine
Standard anesthetic solution administered during routine brachial plexus nerve blockade.
Interventions
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Dexamethasone
Dexamethasone 8 milligrams (liquid) will be added to standard anesthetic solution administered during routine brachial plexus nerve blockade.
Mepivicaine
Standard anesthetic solution administered during routine brachial plexus nerve blockade.
Eligibility Criteria
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Inclusion Criteria
2. ASA I-III
3. Age 18-60
4. BMI \< 35
Exclusion Criteria
2. Contra-indication to regional anesthesia/ supraclavicular brachial plexus blockade e.g. bleeding diathesis, coagulopathy.
3. Peripheral neuropathy.
4. Peptic ulcer disease.
5. Diabetes Mellitus.
6. Inability to give informed consent.
18 Years
60 Years
ALL
No
Sponsors
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University Health Network, Toronto
OTHER
Responsible Party
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University Health Network
Locations
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Toronto Western Hospital, University Health Network
Toronto, Ontario, Canada
Countries
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Other Identifiers
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08-0896-B
Identifier Type: -
Identifier Source: org_study_id
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