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临床试验/NCT01742845
NCT01742845已完成不适用

Ultrasound-guided Intermediate Cervical Block Versus Superficial Cervical Block for Carotid : a Randomised Controlled Trial

Centre Hospitalier Universitaire de Besancon2 个研究点 分布在 1 个国家目标入组 86 人开始时间: 2011年4月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
86
试验地点
2
主要终点
cervical block success

研究概览

简要总结

The aim of this prospective, randomised, controlled study is to compare the efficacy of ultrasound-guided intermediate cervical block to superficial block for carotid endarterectomy.

Patients scheduled for carotide endarterectomy under regional anaesthesia (ropivacaine 4.75 mg/ml) are randomised into 2 groups according to the technique of anaesthesia performed: superficial cervical block (Control group) or, ultrasound guided intermediate cervical block (Echo group). Main outcome is cervical block success, defined by surgery performed under regional anaesthesia without supplemental topical lidocaine. Secondary outcomes are rate of conversion to general anaesthesia, total dose of supplemental topical lidocaine and block-related complications.

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
Single (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

入选标准

  • patient scheduled for elective carotid artery endarterectomy under regional anaesthesia

排除标准

  • indication for general anaesthesia
  • known bleedind diathesis
  • past medical allergy to local anaesthesic
  • severe chronic pulmonary disease
  • contralateral diaphragmatic motion abnormalities
  • previous cervical ipsilateral surgery
  • age < 18 years

结局指标

主要结局

cervical block success

时间窗: surgery time

carotid artery endarterectomy performed under regional anaesthesia without supplemental topical lidocaine.

次要结局

  • percentage of conversion to general anaesthesia(surgery time)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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