Carotid Atherosclerosis Clinical Trial
Official title:
Ultrasound-guided Intermediate Cervical Block Versus Superficial Cervical Block for Carotid : a Randomised Controlled Trial
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.
n/a
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Supportive Care
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