Comparison of Central Versus Peripheral Placement of Local Anesthetic
NCT ID: NCT00699244
Last Updated: 2017-06-12
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
218 participants
INTERVENTIONAL
2006-12-31
2009-03-31
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
NONE
Study Groups
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Peripheral placement of local anesthesia
to receive ultrasound guided peripheral placement of local anesthetic
Peripheral placement of local anesthesia
Peripheral placement of local anesthesia
Central placement of local anesthesia
to receive central placement of local anesthetic
Central placement of local anesthesia
Central placement of local anesthesia
Interventions
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Peripheral placement of local anesthesia
Peripheral placement of local anesthesia
Central placement of local anesthesia
Central placement of local anesthesia
Eligibility Criteria
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Inclusion Criteria
* Patient is undergoing elective hand or forearm surgery.
* Patient is an adult, 18 years old or older.
Exclusion Criteria
* Patient unable to cooperate.
* Patient with a known brachial plexus injury.
* Medical contraindication to anesthetic technique (allergy, cardiac condition, neurologic condition, localized infection, bleeding disorder).
* Patients who are pregnant.
18 Years
ALL
No
Sponsors
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Vanderbilt University
OTHER
Responsible Party
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Clifford Bowens
Assistant Professor
Principal Investigators
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Locations
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Vanderbilt University Orthopedic Surgicenter
Nashville, Tennessee, United States
Countries
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Related Links
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Vanderbilt University Medical Center Department of Anesthesiology
Other Identifiers
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61267
Identifier Type: -
Identifier Source: org_study_id
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