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Clinical Trial Summary

The primary objective of this pilot study is to assess the feasibility of comparing two standardized approaches to manage post-operative pain following spine surgery: one approach using Patient Controlled Analgesia (PCA) devices to deliver opioid analgesics, and the other approach using EXPAREL® infiltration at the site of surgery and nurse-administered opioid analgesics.


Clinical Trial Description

The study will assess the feasibility of the methods proposed, including recruitment, eligibility, standardization of both post-operative pain management approaches, and assessment of clinical, hospital efficiency, medication use, health services use, and economic outcomes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03076710
Study type Observational
Source University of Miami
Contact
Status Withdrawn
Phase
Start date July 31, 2017
Completion date March 2022

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