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临床试验/NCT04446403
NCT04446403Unknown不适用

Analgesic Effect of Ultrasound Guided Combined (Suprascapular and Circumflex Nerve Blocks ) Versus (Suprascapular Nerve and Posterior Cord Nerve Blocks at Infraclavicular Level ) During Shoulder Arthroscopy : A Randomized Controlled Study

Bassant M. Abdelhamid2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2020年6月25日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
30
试验地点
2
主要终点
Time of the first postoperative analgesic request

研究概览

简要总结

Shoulder arthroscopy is associated with severe postoperative pain. Traditionally, the interscalene approach to the brachial plexus has been employed to manage postoperative pain following shoulder surgery.To provide more complete shoulder joint analgesia, suprascabular nerve block (SSNB) was combined with block of the circumflex nerve which comes from the posterior cord of the brachial plexus that usually gives also upper subscapular, thoracodorsal, lower subscapular and radial nerves.

详细描述

Aim of the work is to compare postoperative analgesic effect of ultrasound guided combined suprascapular and circumflex nerve blocks versus suprascapular nerve and posterior cord blocks at infraclavicular level .

Thirty four patients aged from 18-70 years old, with ASA physical status I-II-III and scheduled for shoulder surgeries will be included in the study. Patients will be randomly allocated using computer-generated table into one of two groups:

  • Group circumflex → will undergo ultrasound guided SSN+circumflex.
  • Group posterior cord → will undergo ultrasound guided SSN+posterior cord.

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, Care Provider, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • ASA I-II.-III
  • Undergoing shoulder arthroscopy.

排除标准

  • Patient refusal
  • Known allergy to local anesthetics
  • Bleeding disorders
  • Inability to provide informed consent

结局指标

主要结局

Time of the first postoperative analgesic request

时间窗: 12 hours postoperative

次要结局

  • Visual analogue score(12 hours postoperative)
  • Total morphine consumption(12 hours postoperative)

研究者

发起方
Bassant M. Abdelhamid
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Bassant M. Abdelhamid

associate professor

Cairo University

研究点 (2)

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