Abstract | BACKGROUND: METHODS: Open trial was carried out on different dosage schedules of lornoxicam (4 or 8 mg bid and 4mg tid) administered for six to twelve months. Patients of both sexes were enrolled, with classical or definite rheumatoid arthritis according to the A.R.A. criteria. RESULTS: Thirty-four patients (28 F, 6 M) were admitted, mean age (+/- SD) 53.9+/-14.2 years, mean duration of illness 9.2+/-10.7 years. Lornoxicam 8-16 mg/day showed good safety and therapeutic activity in long term treatment. Clinical improvement was limited, but progression of the disease was controlled. No adverse events were complained. CONCLUSIONS:
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Authors | L Frizziero, M C Focherini, M Valentini, M Reta, P Rocchi |
Journal | Minerva medica
(Minerva Med)
Vol. 93
Issue 4
Pg. 315-20
(Aug 2002)
ISSN: 0026-4806 [Print] Italy |
Vernacular Title | Studio a lungo termine su efficacia e sicurezza terapeutica di lornoxicam nell'artrite reumatoide. |
PMID | 12207202
(Publication Type: Clinical Trial, English Abstract, Journal Article)
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Chemical References |
- Anti-Inflammatory Agents, Non-Steroidal
- Piroxicam
- lornoxicam
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Topics |
- Adult
- Aged
- Anti-Inflammatory Agents, Non-Steroidal
(therapeutic use)
- Arthritis, Rheumatoid
(drug therapy)
- Female
- Humans
- Male
- Middle Aged
- Piroxicam
(analogs & derivatives, therapeutic use)
- Time Factors
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