Jaegemann V, Kolb E, Pabst J, Lataste X
Arzneimittelforschung. 1981;31(5a):929-31.
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.
对59例患有中度严重至重度拉伤和扭伤的患者进行了一项双盲随机试验,以比较4-(对氟苯基)-1-异丙基-7-甲基-2(1H)-喹唑啉酮(氟丙喹宗)缓解疼痛的疗效。患者每天接受50毫克或100毫克氟丙喹宗,最多6次,持续3天。主观评估结果显示,2天后所有患者的疼痛要么完全缓解,要么明显改善。两种治疗方法在第1天和第2天后缓解自发疼痛和运动疼痛方面同样有效。两组患者对治疗的总体评价或医生对治疗反应的评估没有差异。在短期试验中,两种剂量的耐受性都很好。