Continuous Blockade of the Brachial Plexus

Status Completed

Clinical Trial Summary

This study will answer the question whether there is a difference in the effects and complication rates of ultrasound guided continuous interscalene block (CISB) and nerve stimulation-guided continuous cervical paravertebral block (CCPVB). The aim of this study is to evaluate the differences in efficacy and side effects - if any.

Clinical Trial Description

This is a prospective randomized double-blinded study that will compare two commonly used approaches for the continuous blockade of the brachial plexus: the CCPVB, which focusses on the six cervical nerve root (C6 root), and CISB, which focuses on the upper trunk of the brachial plexus. Data of sensory testing, motor strength, shoulder pain, phrenic nerve function, recurrent laryngeal nerve (RNL) function, ipsilateral Horner's syndrome, block time and medication doses used for block placement, will be collected. All observations and measurements will be made by a member of the research team who is unaware of patient allocation to any particular group. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT02769429
Study type	Observational
Source	University of Florida
Contact
Status	Completed
Phase
Start date	September 19, 2016
Completion date	September 26, 2018

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