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Clinical Trial Summary

To determine the efficacy and safety of oxycodone i.v. patient-controlled analgesia (PCA) in the pain relieving treatment during 48h postoperative period, by comparing with morphine i.v. PCA.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01304134
Study type Interventional
Source Mundipharma (China) Pharmaceutical Co. Ltd
Contact
Status Completed
Phase Phase 3
Start date March 2010
Completion date August 2010

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