Patient Preferences, Analgesic Delivery Method and Pain Reduction in Spine Patients
Status:
Withdrawn
Trial end date:
2019-06-01
Target enrollment:
Participant gender:
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.