Coto V, Oliviero U, Cocozza M, Milani M
Department of Internal Medicine, University of Naples, Italy.
J Int Med Res. 1998 Aug-Sep;26(4):200-5. doi: 10.1177/030006059802600404.
In a controlled, randomized, 6-year trial the safety and efficacy of picotamide, a dual-action antithromboxane agent, were assessed in 50 patients with type 2 diabetes mellitus at increased risk of thrombotic vascular events. The patients were randomized to two groups of equal size and received 900 mg picotamide daily or placebo. After phase I (double-blind; years 1 - 2), patients receiving placebo were treated, if necessary, with antiplatelet drugs (aspirin, ticlopidine) while members of the other group continued to receive 600 mg picotamide daily. In the course of the study 21 vascular events occurred: 16 in the group receiving placebo (fatal myocardial infarction, n = 7; non-fatal stroke, n = 3) and five in the group receiving drug (fatal myocardial infarction, n = 2) (P < 0.005; Fisher's exact test). One patient (placebo group) died of malignant disease. During the initial double-blind phase a total of nine vascular events was observed (six and three in the groups receiving placebo and drug, respectively). Picotamide treatment was well tolerated and no major side-effects were observed during the study periods.
在一项为期6年的对照随机试验中,对50名有血栓性血管事件高风险的2型糖尿病患者评估了双重作用抗血栓素药物匹可托安的安全性和有效性。患者被随机分为两组,每组人数相等,分别每日服用900毫克匹可托安或安慰剂。在第一阶段(双盲;第1 - 2年)后,若有必要,接受安慰剂的患者用抗血小板药物(阿司匹林、噻氯匹定)治疗,而另一组患者继续每日服用600毫克匹可托安。在研究过程中发生了21起血管事件:接受安慰剂组16起(致命性心肌梗死7例;非致命性中风3例),接受药物组5起(致命性心肌梗死2例)(P<0.005;Fisher精确检验)。1名患者(安慰剂组)死于恶性疾病。在最初的双盲阶段共观察到9起血管事件(接受安慰剂组和药物组分别为6起和3起)。匹可托安治疗耐受性良好,在研究期间未观察到重大副作用。