Acheson J, Danta G, Hutchinson E C
Br Med J. 1969 Mar 8;1(5644):614-5. doi: 10.1136/bmj.1.5644.614.
A controlled double-blind study of the effect of dipyridamole was performed in 169 patients with established cerebral vascular disease. A dose of 400 mg. was used initially, given daily for an average of 14 months; the dose was then increased to 800 mg. daily for a further average period of 11 months. When the incidence of cerebral ischaemic episodes during treatment was compared in the drug-treated and placebo-treated groups no significant difference was found.
对169例已确诊的脑血管疾病患者进行了一项关于双嘧达莫疗效的对照双盲研究。初始剂量为400毫克,每日服用,平均服用14个月;然后剂量增加至每日800毫克,再平均服用11个月。比较药物治疗组和安慰剂治疗组在治疗期间脑缺血发作的发生率,未发现显著差异。