NCT01263652

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

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

• Status: Withdrawn
• Phase: N/A
• Study type: Interventional
• Enrollment: 0 (actual)
• Sponsor: Western Galilee Hospital-Nahariya · Other Government
• Sex: All
• Age: 15 Years – 100 Years
• Healthy volunteers: Not accepted

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.

Conditions

• Pain Relief

Interventions

Type	Name	Description
DRUG	Diclofenac hydroxyethylpyrrolidine	IM/PO
DRUG	orphenadrine	IM/PO orphenadrine
DRUG	Tramadol	IM/PO tramadol
DRUG	Dipyrone	PO/IM Dipyrone

Timeline

• Start date: 2010-12-31
• Primary completion: 2019-06-01
• Completion: 2019-06-01
• First posted: 2010-12-21
• Last updated: 2020-05-27