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Postoperative subQ Pain Control for Spinal Fusion Surgery

Surgery Clinical Trial

Official title:
Postoperative subQ Pain Control for Spinal Fusion Surgery

Clinical Trial Summary

Post-operative pain following lumbar spine fusion is frequently difficult to manage and can lead to increased doses of opiate pain medications to control pain. In this study, the use of subcutaneous local anesthesia will be studied to determine its efficacy at reducing post-operative pain following spinal fusion surgery.

Clinical Trial Description

For patients randomized to the experimental or to the placebo groups, two subcutaneous catheters will be tunneled under the skin with large hollow-bore needles along the entire length of the incision on either side prior to closure. These catheters will deliver study drug (0.25% Marcaine) directly into the incision. They will be affixed to the skin with steri-strips. The catheters will then be attached to a drug delivery pump at 2mL/hour and will be removed prior to discharge. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03476811
Study type Interventional
Source University of Arizona
Contact
Status Completed
Phase Phase 2
Start date February 9, 2018
Completion date June 30, 2021
View Details
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