drugset / Trial / NCT01263652
Patient Preferences, Analgesic Delivery Method and Pain Reduction in Spine Patients
Withdrawn
Western Galilee Hospital-Nahariya
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Diclofenac epolamine | Unknown | — | Intramuscular |
| Comparator | Orphenadrine | Small molecule | — | Intramuscular |
| Comparator | Tramadol | Other / unclassified | — | Intramuscular |
| Comparator | dipyrone | Unknown | — | Intramuscular |
Indications
No indication recorded.