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Postoperative Analgesia in Laminectomy — (PAL)  

Postoperative Pain Clinical Trial

Official title:
The Effect of Naproxen Sodium + Codeine, and Paracetamol+ Codeine on Postoperative Laminectomy Pain

Clinical Trial Summary

Compare the analgesic effects of naproxen sodium codeine, paracetamol codeine and placebo on postoperative pain and tramadol (Contramal) consumption during the first 24 hour after a lumbar disk surgery.

Clinical Trial Description

Compare the analgesic effects of naproxen sodium codeine paracetamol codeine and placebo on postoperative pain intensity measured by the visual analogue scale, and evaluated tramadol consumption and related side effects. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02255955
Study type Interventional
Source Diskapi Yildirim Beyazit Education and Research Hospital
Contact Reyhan Polat, MD
Phone +905326734310
Email reyhanp9@gmail.com
Status Not yet recruiting
Phase Phase 4
Start date October 2014
Completion date December 2014
View Details
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