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临床试验/NCT01589354
NCT01589354Unknown不适用

Effectiveness of Interscalene Brachial Plexus Block and Intra-articular Injection of Ropivacaine for Post-operative Analgesia in Arthroscopic Shoulder Stabilization Surgery

NHS Grampian0 个研究点目标入组 60 人开始时间: 2012年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
发起方
NHS Grampian
入组人数
60
主要终点
Mean pain score over the first 24 hours following arthroscopic shoulder stabilisation operation

研究概览

简要总结

This study evaluates two anaesthetic techniques namely interscalene brachial plexus block and intra-articular local anaesthetic injection. Both techniques are currently used for providing postoperative pain relief following arthroscopic shoulder stabilisation operation. It will be a randomised controlled trial involving 30 patients in two groups.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • All adult patients above the age of 18 years undergoing arthroscopic shoulder stabilisation operation

排除标准

  • Patients not meeting inclusion criteria
  • Patients unable to give informed consent
  • Patient refusal to participate in the study
  • Contraindications to Interscalene block
  • Allergy to local anaesthetics
  • Peripheral neuropathy from any cause
  • Patients on opiates for chronic pain
  • Pregnant women

研究组 & 干预措施

Interscalene brachial plexus block

Experimental

干预措施: Interscalene brachial plexus block (Procedure)

Interscalene brachial plexus block

Experimental

干预措施: Ultrasound guided technique (Device)

Interscalene brachial plexus block

Experimental

干预措施: Ropivacaine (Drug)

Intra-articular injection

Experimental

干预措施: Intra-articular Ropivacaine injection (Procedure)

Intra-articular injection

Experimental

干预措施: Ropivacaine (Drug)

结局指标

主要结局

Mean pain score over the first 24 hours following arthroscopic shoulder stabilisation operation

时间窗: 24 months

次要结局

  • Post-operative analgesic requirements in the first 24 hours after surgery(24 months)
  • Patient assessment of quality of analgesia and identifying any complications as a result of the two anaesthetic procedures(24 months)

研究者

发起方
NHS Grampian
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Amr M Mahdy

Dr

NHS Grampian

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