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A double-blind trial of feprazone in osteoarthritis of the hip.

Abstract
A double-blind crossover study was carried out in 21 patients with osteoarthrosis of the hip to compare the efficacy and tolerance of feprazone (600 mg/day) and ibuprofen (1200 mg/day), each drug being given for 4 weeks. No statistically significant changes were noted in any of the objective parameters measured, but patients' subjective assessments of pain showed a significant improvement in pain levels (p less than or equal to 0.05, day and night) after feprazone. One patient, who had reported a rash at initial assessment, was withdrawn at the end of the first treatment period (on feprazone) when he developed a severe rash, 1 patient was withdrawn because of exacerbation of symptoms (on ibuprofen) and a further patient was lost to follow-up because of intercurrent illness. Both drugs were well tolerated by the other patients and the few side-effects reported were minor in nature.
AuthorsL S Bain, M P Lynch, G M Bruce
JournalCurrent medical research and opinion (Curr Med Res Opin) Vol. 4 Issue 9 Pg. 665-9 ( 1977) ISSN: 0300-7995 [Print] England
PMID338255 (Publication Type: Clinical Trial, Comparative Study, Controlled Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • Feprazone
  • Phenylbutazone
  • Ibuprofen
Topics
  • Aged
  • Clinical Trials as Topic
  • Double-Blind Method
  • Female
  • Feprazone (adverse effects, therapeutic use)
  • Hip Joint
  • Humans
  • Ibuprofen (adverse effects, therapeutic use)
  • Male
  • Middle Aged
  • Osteoarthritis (drug therapy)
  • Pain
  • Phenylbutazone (analogs & derivatives)

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