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Anesthetic to Reduce Dysphagia After Anterior Cervical Discectomy and Fusion Surgery

Dysphagia Clinical Trial

Official title:
The Effectiveness of Postoperative Local Retropharyngeal Space Anesthetic to Reduce Dysphagia After Anterior Cervical Discectomy and Fusion Surgery

Clinical Trial Summary

The main objective of this study is to analyze the effects of local anesthetic application into the retropharyngeal space and its ability to reduce dysphagia symptoms and/or occurrence rates in patients undergoing anterior cervical discectomy and fusion.

Clinical Trial Description

The patients will be randomly assigned into one of the two groups to receive either bupivacaine hydrochloride 0.5% solution if they are randomized to the treatment group or 0.9% NaCl solution if they are randomized to the control group. These solutions will be poured into the retropharyngeal space intraoperatively before wound closure. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02376205
Study type Interventional
Source Justin Parker Neurological Institute
Contact
Status Completed
Phase N/A
Start date February 2015
Completion date March 11, 2019
View Details
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