Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | naproxen sodium codein | Pain intensity, contramal consumption |
| DRUG | paracetamol codein | Pain intensity, contramal consumption |
| DRUG | Placebo | Pain 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.