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

Phase 4
Conditions
Postoperative Pain, PCA Contramal Consumption
Interventions
Registration Number
NCT02252614
Lead Sponsor
Diskapi Yildirim Beyazit Education and Research Hospital
Brief 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.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
75
Inclusion Criteria
  • American Society of Anesthesiologists 1 or 2 status patients scheduled for elective lumbar disk surgery under general anesthesia
Exclusion Criteria
  • Patients, known allergies to any of the drugs used in this study
  • eptic ulcer disease, hepatic and renal dysfunction, emergency surgery, or inability to provide informed consent (eg, mental disorders)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Naproxen sodium codeinnaproxen sodium codeinPreoperative Naproxen sodium codein administered, pain intensity measured by the visual analogue scale, and contramal consumption and related side effects evaluated.
Paracetamol codeinparacetamol codeinPreoperative paracetamol codein administrered, pain intensity measured by the visual analogue scale, and contramal consumption and related side effects evaluated.
Placebo tabletPlaceboPreoperative placebo tablet administered, pain intensity measured by the visual analogue scale, and contramal consumption and related side effects evaluated.
Primary Outcome Measures
NameTimeMethod
Pain intensity, contramal consumptionPostoperative 24 hour
Secondary Outcome Measures
NameTimeMethod
side effects, nausa, vomitingpostoperative 24 hour
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