Salako L A, Falase A O, Aderounmu A F
Curr Med Res Opin. 1979;6(5):358-63. doi: 10.1185/03007997909109451.
A placebo-controlled, double-blind clinical trial of alprenolol was carried out in 20 hypertensive Africans. The active drug and placebo were each administered for 8 weeks using a crossover design. Alprenolol was given in the form of a slow-release tablet preparation at a dosage of 200 mg twice daily. Four patients were withdrawn from the study either because of side-effects (2 patients) or non-compliance (2 patients). The mean reduction in blood pressure obtained in the 16 patients who completed the trial was less than that usually reported in Caucasians.
对20名非洲高血压患者进行了一项阿普洛尔的安慰剂对照双盲临床试验。采用交叉设计,活性药物和安慰剂各给药8周。阿普洛尔以缓释片剂制剂的形式给药,剂量为每日2次,每次200毫克。4名患者因副作用(2名患者)或不依从性(2名患者)退出研究。完成试验的16名患者的平均血压降低幅度小于通常在白种人中报道的幅度。