drugset / Trial / NCT01263652

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

NCT01263652

RandomizedParallel-groupQuadruple-blindTreatment

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

Drugs

EvaluationDrugModalityDoseRoute
Comparator Diclofenac epolamine Unknown Intramuscular
Comparator Orphenadrine Small molecule Intramuscular
Comparator Tramadol Other / unclassified Intramuscular
Comparator dipyrone Unknown Intramuscular

Indications

No indication recorded.