Comparison of Pulmonary Function and Efficacy of Different Nerve Block Catheters for Shoulder Surgery
NCT ID: NCT02117778
Last Updated: 2017-02-03
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
75 participants
INTERVENTIONAL
2014-03-31
2015-01-31
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
DOUBLE
Study Groups
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Interscalene
Continuous Interscalene Nerve Block
Continuous Nerve Block
Supraclavicular
Continuous Supraclavicular Nerve Block
Continuous Nerve Block
Suprascapular
Continuous Suprascapular Nerve Block
Continuous Nerve Block
Interventions
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Continuous Nerve Block
Eligibility Criteria
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Inclusion Criteria
* ASA physical status I-III
* \>18 years old
* Non-pregnant (or lactating)
* Consent to participate in the study
Exclusion Criteria
* \< 18 years old
* Chronic opioid use
* Localized infection
* Pregnancy or lactating
* Pre-existing coagulopathy
* Allergy to ultrasound gel or local anesthetics
* Diaphragmatic dysfunction
18 Years
ALL
No
Sponsors
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Benaroya Research Institute
OTHER
Responsible Party
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Principal Investigators
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David Auyong, MD
Role: PRINCIPAL_INVESTIGATOR
Physician
Locations
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Virginia Mason Medical Center
Seattle, Washington, United States
Countries
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Other Identifiers
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BRI IRB13086
Identifier Type: -
Identifier Source: org_study_id
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