Pain control after dental surgery: a double-blind, randomised trial of lornoxicam versus morphine
Authors:
- Steen Sindet-PedersenSSSteen Sindet-Pedersen
- Ulla LarsenULUlla Larsen
- Ulla BangUBUlla Bang
- Janne IngerslevJIJanne Ingerslev
- Ove NielsenONOve Nielsen
- Hans Jørgen HansenHHHans Jørgen Hansen
- Annette Kjær ErsbøllAEAnnette Kjær Ersbøll
- 1 October 1996
- journal article
- clinical trial
- Published by Wolters Kluwer Health in Pain
- Vol. 67 (2) , 335-343
Abstract
Lornoxicam is a new non-steroidal anti-inflammatory drug of the oxicam class. This randomised, double-blind, placebo controlled trial compared the analgesic efficacy and tolerability of intramuscular (IM) injections of lornoxicam (4, 8, 16 and 20 mg) with morphine (10 and 20 mg) and placebo in 252 patients with mainly moderate to severe pain following surgical removal of an impacted mandibular third molar. Patients treated with lornoxicam or morphine experienced a significantly greater cumulative pain relief over the 4-h post-injection period (TOTPAR0-4) than placebo recipients. This effect appeared to be dose-dependent, with patients in the lornoxicam 4 mg or morphine 10 mg groups recording significantly lower TOTPAR0-4 scores than patients in the higher dosage groups of these drugs. No significant difference was detected between the morphine 20 mg group and the lornoxicam 8, 16 and 20 mg groups. Lornoxicam was well tolerated at all doses and was associated with a significantly lower incidence of adverse events than morphine 10 or 20 mg. Thus, the analgesic efficacy of IM lornoxicam at doses > or = 4 mg is superior to placebo, and doses > or = 8 mg are at least as effective as IM morphine 20 mg. Furthermore, lornoxicam possesses a more favourable tolerability profile than morphine and thus represents an attractive alternative for the treatment of moderate to severe acute pain.Keywords
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