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UnknownNCT02252614

Efficacy of Intravenous Naproksen Sodium+Codein and Paracetamol+Codein on Postoperative Pain on Postoperative Pain

Efficacy of Intravenous Naproksen Sodium+Codein and Paracetamol+Codein on Postoperative Pain and Contramal Consumption After a Lumbar Disk Surgery

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 – 90 Years
Healthy volunteers
Not accepted

Summary

Comparition the analgesic effects of intravenous naproksen sodyum+codein with that of paracetamol+codein on postoperative pain and contramal consumption during the first 24 hour after a lumbar disk surgery.

Detailed description

Patients were treated using patient-controlled analgesia with contramal for 24 hours after a lumbar disk surgery and randomized to receive IV naproksen sodium+codein, paracetamol+codein or isotonic saline (placebo). The primary endpoint was pain intensity measured by the visual analogue scale, and secondary endpoints were contramal consumption and related side effects.

Conditions

Interventions

TypeNameDescription
DRUGnaproxen sodium codeinPain intensity, contramal consumption
DRUGparacetamol codeinPain intensity, contramal consumption
DRUGPlaceboPain intensity, contramal consumption

Timeline

Start date
2014-09-01
Primary completion
2014-12-01
Completion
2014-12-01
First posted
2014-09-30
Last updated
2014-09-30

Source: ClinicalTrials.gov record NCT02252614. Inclusion in this directory is not an endorsement.

Efficacy of Intravenous Naproksen Sodium+Codein and Paracetamol+Codein on Postoperative Pain on Postoperative Pain (NCT02252614) · Clinical Trials Directory