Andersson P G, Hinge H H, Johansen O, Andersen C U, Lademann A, Gøtzsche P C
Department of Neuromedicine, Hjørring Sygehus, Denmark.
Cephalalgia. 1989 Mar;9(1):29-32. doi: 10.1046/j.1468-2982.1989.0901029.x.
Naproxen was compared with placebo in a double-blind, crossover trial in classic and common migraine. The trial was terminated at a fixed date; 37 patients had entered, 5 of whom were excluded. Naproxen was given as 750 mg at the first symptom of the attack, a total of 1250 mg per 24 h was allowed. Patients were followed for six attacks or three months in each phase, whichever came first. The severity of the headache was significantly less with naproxen in the first 2 h of the attack (p = 0.047), whereas there was no difference when the whole attack was considered. Significantly more patients preferred naproxen (p = 0.042). Side effects occurred in five patients, causing withdrawal of one patient while on naproxen.
在一项针对典型偏头痛和普通偏头痛的双盲交叉试验中,对萘普生与安慰剂进行了比较。该试验在固定日期终止;37名患者入组,其中5名被排除。在发作的第一个症状出现时给予萘普生750mg,每24小时允许总量为1250mg。在每个阶段,对患者随访六次发作或三个月,以先达到者为准。在发作的前2小时,使用萘普生时头痛的严重程度明显较轻(p = 0.047),而考虑整个发作时则没有差异。明显更多的患者更喜欢萘普生(p = 0.042)。五名患者出现副作用,一名患者在服用萘普生时停药。