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Fluproquazone in the management of strains and sprains.

Abstract
A double-blind randomized trial was carried out in 59 patient suffering from moderately severe to severe strains and sprains to compare the efficacy of 4-(p-fluorophenyl)-1-isopropyl-7-methyl-2(1H)-quinazolinone (fluproquazone) in the relief of pain. Patients received either 50 mg or 100 mg fluproquazone up to 6 times daily for 3 days. The results of subjective assessments showed that after 2 days pain had either completely resolved or markedly improved in all patients. Both treatments were equally effective in relieving both spontaneous pain and pain on movement after 1 and 2 days. No differences were found between the two groups in the patients' overall evaluation of treatment or physicians' assessment of therapeutic response. Both dosage were well tolerated during the short-term trial.
AuthorsV Jaegemann, E Kolb, J Pabst, X Lataste
JournalArzneimittel-Forschung (Arzneimittelforschung) Vol. 31 Issue 5a Pg. 929-31 ( 1981) ISSN: 0004-4172 [Print] Germany
PMID6973989 (Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
Chemical References
  • Anti-Inflammatory Agents, Non-Steroidal
  • Placebos
  • Quinazolines
  • Quinazolinones
  • fluproquazone
Topics
  • Adult
  • Anti-Inflammatory Agents, Non-Steroidal (therapeutic use)
  • Double-Blind Method
  • Female
  • Humans
  • Male
  • Middle Aged
  • Placebos
  • Quinazolines (therapeutic use)
  • Quinazolinones
  • Sprains and Strains (drug therapy)

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