跳至主要内容
临床试验/NCT04364542
NCT04364542Unknown不适用

Suprascapular Nerve Block Efficacy for Arthroscopic Rotator Cuff Repair: a Randomized Clinical Trial

Ivan Simionato2 个研究点 分布在 1 个国家目标入组 98 人开始时间: 2020年5月10日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
98
试验地点
2
主要终点
Pain intensity: Numeric Pain Rating Scale

研究概览

简要总结

This study evaluates the analgesia induced by suprascapular nerve block in comparison to interscalene nerve block in arthroscopic rotator cuff repairs. The experimental and the control group will receive the suprascapular nerve block and interscalene nerve block, respectively.

详细描述

Peripheral nerve blocks are widely used for postsurgical analgesia. Interscalene nerve block provides a total brachial plexus motor and sensitive blockade while the suprascapular nerve block produces only a specific peripheral blockade.

The interscalene nerve block is the most frequently used anesthesia technique and requires a longer learning curve. Complications related to this technique may be more severe and frequent in comparison to other regional anesthesia techniques.

The suprascapular nerve block yields less adverse effects, discomfort and rebound effect as this technique does not completely block the upper limb motor 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
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

Triple (Participant, Investigator, and Outcomes Assessor)

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age between 18 and 80 years old
  • Confirmed rotator cuff tear by magnetic resonance imaging

排除标准

  • Irreparable cuff tears (retracted lesions to the glenoid rim and/or fourth grade fatty infiltration)
  • Partial repair of cuff tears (immobile lesions)
  • Rheumatic diseases
  • Neck-related shoulder pain
  • Glenohumeral instability or osteoarthritis

结局指标

主要结局

Pain intensity: Numeric Pain Rating Scale

时间窗: 72 hours after surgery

Numeric Pain Rating Scale - no pain (0), unbearable pain (10)

次要结局

  • Opiate Consumption(Postoperative hours 1-72)

研究者

发起方
Ivan Simionato
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Ivan Simionato

Clinical Researcher

Shoulder Surgery Group, Santa Casa de Porto Alegre

研究点 (2)

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