Comparison of Pulmonary Function and Efficacy of Different Nerve Block Catheters for Shoulder Surgery

NCT ID: NCT02117778

Last Updated: 2017-02-03

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

75 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-03-31

Study Completion Date

2015-01-31

Brief Summary

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This study is designed to evaluate lung function and pain control of continuous supraclavicular versus suprascapular versus interscalene nerve catheters in subjects undergoing total shoulder replacement. The investigators hypothesize that all three groups would have similar pain control; the supraclavicular and suprascapular groups may have better lung function.

Detailed Description

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Conditions

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Post-Operative Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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Interscalene

Continuous Interscalene Nerve Block

Group Type ACTIVE_COMPARATOR

Continuous Nerve Block

Intervention Type PROCEDURE

Supraclavicular

Continuous Supraclavicular Nerve Block

Group Type ACTIVE_COMPARATOR

Continuous Nerve Block

Intervention Type PROCEDURE

Suprascapular

Continuous Suprascapular Nerve Block

Group Type ACTIVE_COMPARATOR

Continuous Nerve Block

Intervention Type PROCEDURE

Interventions

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Continuous Nerve Block

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Unilateral total shoulder arthroplasty
* ASA physical status I-III
* \>18 years old
* Non-pregnant (or lactating)
* Consent to participate in the study

Exclusion Criteria

* Refusal to participate
* \< 18 years old
* Chronic opioid use
* Localized infection
* Pregnancy or lactating
* Pre-existing coagulopathy
* Allergy to ultrasound gel or local anesthetics
* Diaphragmatic dysfunction
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Benaroya Research Institute

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Countries

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United States

Other Identifiers

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BRI IRB13086

Identifier Type: -

Identifier Source: org_study_id

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