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
| Type | Name | Description |
|---|---|---|
| DRUG | bupivacaine hydrochloride 0.5% solution | 10mL will be poured into the retropharyngeal space intraoperatively during anterior cervical discectomy and fusion procedure |
| DRUG | 0.9% NaCl solution | 10mL 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.