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临床试验/NCT03224884
NCT03224884已完成不适用

A Randomized Comparison Between Interscalene and Supraclavicular Brachial Plexus Blocks For Arthroscopic Shoulder Surgery

University of Chile2 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2017年7月24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
发起方
入组人数
44
试验地点
2
主要终点
Static pain at 30 minutes after arrival in the PACU

研究概览

简要总结

Interscalene brachial plexus block constitutes the analgesic criterion standard for shoulder surgery. However it is associated with a high incidence of hemidiaphragmatic paralysis (HDP) that may not be tolerated by patients with chronic pulmonary disease.

This randomized controlled trial will compare ultrasound-guided interscalene block (ISB) and supraclavicular block in patients undergoing arthroscopic shoulder surgery.

The main outcome is static pain at 30 minutes after arrival in the post anesthesia care unit (PACU) as measured by a numerical rate scale (NRS) from 0 to 10.

Our research hypothesis is that interscalene and supraclavicular blocks will result in equivalent postoperative analgesia at 30 minutes in the PACU. The equivalence margin is set at 2 points

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Triple (Participant, Care Provider, 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

  • Patients undergoing arthroscopic shoulder surgery
  • American Society of Anesthesiologists classification 1-3
  • Body mass index between 20 and 35

排除标准

  • Adults who are unable to give their own consent
  • Pre-existing neuropathy
  • Coagulopathy
  • Obstructive or restrictive pulmonary disease
  • Renal failure
  • Hepatic failure
  • Allergy to local anesthetics
  • Pregnancy
  • Prior surgery in the corresponding side of the neck or supraclavicular fossa
  • Chronic pain syndromes requiring opioid intake at home

研究组 & 干预措施

Interscalene block

Active Comparator

Patients randomized to receive an interscalene block .

干预措施: Interscalene block (Procedure)

Supraclavicular block

Experimental

Patients randomized to receive a supraclavicular block.

干预措施: Supraclavicular block (Procedure)

结局指标

主要结局

Static pain at 30 minutes after arrival in the PACU

时间窗: 30 minutes

Evaluated with a NRS from 0 to 10.

次要结局

  • Postoperative static pain at 2 hours(2 hours)
  • Postoperative static pain at 12 hours(12 hours)
  • Postoperative static pain at 24 hours(24 hours)
  • Incidence of HDP at 30 minutes after interscalene or supraclavicular block(30 minutes post injection)
  • Incidence of complete block(30 minutes post injection)
  • Procedural pain during blocks(1 hour before surgery)
  • Postoperative opioid consumption(24 hours after surgery)
  • Static pain at 60 minutes after arrival in the PACU(60 minutes)
  • Postoperative static pain at 3 hours(3 hours)
  • Postoperative static pain at 6 hours(6 hours)
  • Block performance time(1 hour before surgery)
  • Block- and opioid-related side effects(1 week)
  • Sensory and Motor block(30 minutes post injection)
  • Incidence of HDP at 30 minutes after arrival to PACU.(30 minutes after arrival to PACU)
  • Onset time(1 hour before surgery)
  • Intraoperative opioid requirements(Intraoperative period)
  • Patient satisfaction(24 hours after surgery)
  • Surgical duration(intraoperative period)

研究者

发起方
University of Chile
申办方类型
Other
责任方
Principal Investigator
主要研究者

Julian Aliste

Clinical Instructor

University of Chile

研究点 (2)

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