Clinical Trials Directory

Trials / Unknown

UnknownNCT02255955

Postoperative Analgesia in Laminectomy

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

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
75 (estimated)
Sponsor
Diskapi Yildirim Beyazit Education and Research Hospital · Other Government
Sex
All
Age
16 Years – 85 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUG550 mg naproxen sodium and 30mg codeinePostoperative contramal consumption, pain intensity, side effects
DRUG300 mg paracetamol and 30 mg codeinePostoperative contramal consumption, pain intensity, side effects
DRUGplacebo tabletPostoperative contramal consumption, pain intensity, side effects

Timeline

Start date
2014-10-01
Primary completion
2014-12-01
Completion
2014-12-01
First posted
2014-10-03
Last updated
2014-12-30

Source: ClinicalTrials.gov record NCT02255955. Inclusion in this directory is not an endorsement.