Rosenthal M
Curr Med Res Opin. 1984;9(5):304-9. doi: 10.1185/03007998409109597.
Fifty patients suffering from acute soft tissue rheumatism entered an open parallel group study of flurbiprofen 200 mg to 400 mg daily versus piroxicam 20 mg to 40 mg daily for 4 weeks. Both treatments caused statistically significant improvements in pain, pain on active movement, restriction of passive movement and reduction of strength. Global assessments of the patients' progress also improved significantly with both compounds. Flurbiprofen was significantly superior to piroxicam with regard to relief of pain at Day 28, pain on active movement at Days 14 and 28, pain on passive movement at Days 7, 14 and 28 and pain, as measured by a visual analogue scale, at Day 14. Clinically, flurbiprofen showed greater improvements in all the other parameters throughout the study period. Side-effects, mainly gastro-intestinal in nature, occurred in 6 patients receiving flurbiprofen and 8 receiving piroxicam. One patient receiving flurbiprofen was withdrawn due to stomach pain and headache, but no withdrawals due to side-effects were necessary in those receiving piroxicam. One patient receiving piroxicam was withdrawn due to a total remission by Day 14.
50例急性软组织风湿病患者进入一项开放性平行组研究,比较每日服用200毫克至400毫克氟比洛芬与每日服用20毫克至40毫克吡罗昔康,为期4周。两种治疗方法在疼痛、主动运动时疼痛、被动运动受限和力量减弱方面均产生了具有统计学意义的改善。两种药物对患者病情的总体评估也有显著改善。在第28天的疼痛缓解、第14天和第28天的主动运动时疼痛、第7天、第14天和第28天的被动运动时疼痛以及第14天通过视觉模拟量表测量的疼痛方面,氟比洛芬显著优于吡罗昔康。临床上,在整个研究期间,氟比洛芬在所有其他参数方面显示出更大的改善。副作用主要为胃肠道反应,6例接受氟比洛芬治疗的患者和8例接受吡罗昔康治疗的患者出现了副作用。1例接受氟比洛芬治疗的患者因胃痛和头痛退出研究,但接受吡罗昔康治疗的患者中无需因副作用而退出。1例接受吡罗昔康治疗的患者因在第14天完全缓解而退出。