Clinical Trials Directory

Trials / Completed

CompletedNCT02376205

Anesthetic to Reduce Dysphagia After Anterior Cervical Discectomy and Fusion Surgery

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

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
150 (actual)
Sponsor
Justin Parker Neurological Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGbupivacaine hydrochloride 0.5% solution10mL will be poured into the retropharyngeal space intraoperatively during anterior cervical discectomy and fusion procedure
DRUG0.9% NaCl solution10mL will be poured into the retropharyngeal space intraoperatively during anterior cervical discectomy and fusion procedure

Timeline

Start date
2015-02-01
Primary completion
2019-03-11
Completion
2019-03-11
First posted
2015-03-03
Last updated
2020-02-13

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02376205. Inclusion in this directory is not an endorsement.