跳至主要内容
临床试验/NCT02117778
NCT02117778已完成不适用

A Comparative Pulmonary Function Study of Continuous Supraclavicular, Suprascapular, and Interscalene Nerve Catheters After Total Shoulder Arthroplasty

Benaroya Research Institute1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2014年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
75
试验地点
1
主要终点
Lung function

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

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

排除标准

  • •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

研究组 & 干预措施

Interscalene

Active Comparator

Continuous Interscalene Nerve Block

干预措施: Continuous Nerve Block (Procedure)

Supraclavicular

Active Comparator

Continuous Supraclavicular Nerve Block

干预措施: Continuous Nerve Block (Procedure)

Suprascapular

Active Comparator

Continuous Suprascapular Nerve Block

干预措施: Continuous Nerve Block (Procedure)

结局指标

主要结局

Lung function

时间窗: Post-Operative Day 1

Vital Capacity, Spirometry

次要结局

  • Pain(Post Operative Day 1)
  • Opioid Consumption(Post Operative Day 1)
  • Sensory and Motor Function(Post Operative Day 1)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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