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

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.

Timeline

Start

2010-12-31

Primary completion

2019-06-01

Completion

2019-06-01

Outcome

Outcome not reported

Stopped (Enrollment): “inability to complete recruitment as planned”

Drugs

Indications

No indication recorded.