Ketoprofen controlled release (CR) in the treatment of osteoarthrosis; a double blind, randomized multicentre study of single morning versus evening dose
Objective - To compare the morning and evening dose of 200 mg ketoprofen controlled release formulation with regard to both efficacy and GI tolerability. Design - Double-blind, randomized multicentre prospective trial with cross-over design combined with a parallel design. Participants - One hundred...
Gespeichert in:
Veröffentlicht in: | Scandinavian journal of primary health care 1993, Vol.11 (2), p.91-97 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Objective - To compare the morning and evening dose of 200 mg ketoprofen controlled release formulation with regard to both efficacy and GI tolerability.
Design - Double-blind, randomized multicentre prospective trial with cross-over design combined with a parallel design.
Participants - One hundred and eight female and 55 male patients with osteoarthrosis in hip(s) or knee(s) necessitating treatment with nonsteroidal antiinflammatory drugs. Main outcome measure - The degrees of pain and stiffness and joint movement ability in joints with osteoarthrosis.
Results - Both the morning and the evening dose demonstrated a significant effect (p < 0.01) on all efficacy variables. The reduction in degree of pain in the afternoon and in the evening was significantly higher (p < 0.01) for the morning dose. The total frequency and degree of gastrointestinal discomfort increased significantly (p < 0.01) during both treatment periods. The increases were mainly caused by increased gastric pain and constipation. No significant differences were found between the two regimes regarding tolerability.
Conclusion - Ketoprofen controlled release given once daily in the morning compared to the evening to patients with osteoarthrosis may increase the efficacy without reducing the tolerability of the drug. |
---|---|
ISSN: | 0281-3432 1502-7724 |
DOI: | 10.3109/02813439308994909 |