Overview

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

Status:
Withdrawn

Trial end date:
2019-06-01

Target enrollment:
0

Participant gender:
All

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.

Phase:

N/A

Accepts Healthy Volunteers?

Details

Lead Sponsor:

Western Galilee Hospital-Nahariya

Treatments:

Analgesics
Diclofenac
Diclofenac hydroxyethylpyrrolidine
Dipyrone
Orphenadrine
Tramadol

Criteria

Inclusion Criteria:

- Patients with chronic and acute back pain

Exclusion Criteria:

- Recent Spine Surgery