An Interventional Study to Assess the Efficacy and Safety of Oxycodone/Naloxone in Korean Patients With Spinal Disorders
Status:
Completed
Trial end date:
2013-07-01
Target enrollment:
Participant gender:
Summary
Study Objectives:
1. Primary objective
- To assess the pain reduction after 8 weeks treatment from baseline (week 0)
2. Secondary objectives
- To assess the pain reduction after 4 weeks treatment from baseline (week 0)
- To assess the EQ-5D
- To assess physician's overall satisfaction
- To assess subject's overall satisfaction
- To assess safety