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Patient Preferences, Analgesic Delivery Method and Pain Reduction in Spine Patients

Pain Relief Clinical Trial

Official title:
The Relationship Between Patient Preferences, Analgesic Delivery Method and Pain Reduction in Spine Patients

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

Clinical Trial Details
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Status Withdrawn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
View Details
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