Status:
UNKNOWN
Efficacy of Intravenous Naproksen Sodium+Codein and Paracetamol+Codein on Postoperative Pain on Postoperative Pain
Lead Sponsor:
Diskapi Yildirim Beyazit Education and Research Hospital
Conditions:
Postoperative Pain, PCA Contramal Consumption
Eligibility:
All Genders
16-90 years
Phase:
PHASE4
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 su...
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 sa...
Eligibility Criteria
Inclusion
- American Society of Anesthesiologists 1 or 2 status patients scheduled for elective lumbar disk surgery under general anesthesia
Exclusion
- 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)
Key Trial Info
Start Date :
September 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2014
Estimated Enrollment :
75 Patients enrolled
Trial Details
Trial ID
NCT02252614
Start Date
September 1 2014
End Date
December 1 2014
Last Update
September 30 2014
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