Continuous Infraclavicular Nerve Blocks: Needle Versus Catheter Local Anesthetic Bolus
NCT ID: NCT01377545
Last Updated: 2013-01-18
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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WITHDRAWN
PHASE4
INTERVENTIONAL
2013-01-31
2013-01-31
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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Local Anesthetic Via Catheter
30mL of Lidocaine (local Anesthetic) will be injected via a perineural catheter at hour 0.
Local Anesthetic given via perineural catheter for infraclavicular nerve block.
Patients will be randomized to receive 30mL of Lidocaine via Catheter for an infraclavicular nerve block on one side (right or left) and via needle on the other side. Sensory and strength will be tested following local anesthetic administration.
Local Anesthetic Via Needle
30mL of Lidocaine (local Anesthetic) will be injected via a needle at hour 0.
Local Anesthetic given via needle for infraclavicular nerve block
Patients will be randomized to receive 30mL of Lidocaine via Catheter for an infraclavicular nerve block on one side (right or left) and via needle on the other side. Sensory and strength will be tested following local anesthetic administration.
Interventions
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Local Anesthetic given via perineural catheter for infraclavicular nerve block.
Patients will be randomized to receive 30mL of Lidocaine via Catheter for an infraclavicular nerve block on one side (right or left) and via needle on the other side. Sensory and strength will be tested following local anesthetic administration.
Local Anesthetic given via needle for infraclavicular nerve block
Patients will be randomized to receive 30mL of Lidocaine via Catheter for an infraclavicular nerve block on one side (right or left) and via needle on the other side. Sensory and strength will be tested following local anesthetic administration.
Eligibility Criteria
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Inclusion Criteria
* willing to have bilateral infraclavicular blocks/catheters placed
Exclusion Criteria
* opioid use within the previous 4 weeks
* any neuro-muscular deficit of either upper extremity
* body mass index \> 30 kg/m2
* weight \< 50 kg \[100 lbs\]
* pregnancy
* incarceration
18 Years
ALL
Yes
Sponsors
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University of California, San Diego
OTHER
Responsible Party
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Brian M. Ilfeld, MD, MS
Associate Professor, In Residence
Principal Investigators
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Brian M Ilfeld, M.D., M.S.
Role: PRINCIPAL_INVESTIGATOR
University of California, San Diego
Locations
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UCSD CTRI, Hillcrest
San Diego, California, United States
Countries
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Other Identifiers
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Infraclav Needle vs Catheter
Identifier Type: -
Identifier Source: org_study_id
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