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.
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Authors | V Jaegemann, E Kolb, J Pabst, X Lataste |
Journal | Arzneimittel-Forschung
(Arzneimittelforschung)
Vol. 31
Issue 5a
Pg. 929-31
( 1981)
ISSN: 0004-4172 [Print] Germany |
PMID | 6973989
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
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Chemical References |
- Anti-Inflammatory Agents, Non-Steroidal
- Placebos
- Quinazolines
- Quinazolinones
- fluproquazone
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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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