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Pre-emptive Intravenous Analgesia for Elective Inguinal Hernia Repair
NCT01069055Phase 3Unknown
- Sponsor
- Dışkapı Yıldırım Beyazıt Training and Research Hospital
- Start
- Feb 2010
- Primary completion
- Jun 2010
- Modality
- Small Molecules
- Countries
- 1
01
Overview
Phase 3, randomised, double-blind trial in postoperative pain comparing Placebo Control, Lornoxicam and Paracetamol (3 arms). Primary endpoints: Visual Analog Scale for Pain at 48 hours and Morphine consumption at 24 hours. Status: unknown.
02
Drugs
lornoxicamacetaminophen
03
Conditions
postoperative pain
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