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Clinical Trial Summary

The investigators will conduct a randomized double blind study, to determine whether patient analgesic delivery mode preference affects pain reduction quality in non-surgical spine patients.

The patients will receive both intra-muscular and oral non-narcotic analgesics and placebo. During the study period, pain reduction parameters will be collected. At the end of the study period, the investigators will attempt to find a correlation between pre-study patient preferences and the quality of the pain reduction achieved.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01263652
Study type Interventional
Source Western Galilee Hospital-Nahariya
Contact
Status Withdrawn
Phase N/A
Start date December 31, 2010
Completion date June 1, 2019

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