Bennett M B, Helman P, Palmer P
S Afr Med J. 1975 Nov 15;49(49):2036-40.
From 1968 to 1972, a trial of a new agent, drostanolone propionate (Masteril), was conducted. This agent was tested against oophorectomy in a group of premenopausal patients, against nandrolone phenylpropionate (Durabolin) in a perimenopausal group, and against ethinyl oestradiol in a postmenopausal group. In the premenopausal group, 44% responded to Masteril and 22% to oophorectomy. In the perimenopausal group, 34,5% responded to Masteril and 39% to Durabolin. In the postmenopausal group, 57% responded to oestrogens and 38,5% to Masteril. The side-effects of Masteril are generally not serious and rarely contra-indicate its use. Masteril has been shown to be a useful and safe agent for all age groups, even though it may appear to be less effective than oestrogens in the postmenopausal patients.
1968年至1972年,对一种新制剂丙酸屈他雄酮(Masteril)进行了试验。在一组绝经前患者中,将该制剂与卵巢切除术进行对比试验;在一组围绝经期患者中,与苯丙酸诺龙(Durabolin)进行对比试验;在一组绝经后患者中,与炔雌醇进行对比试验。在绝经前组中,44%的患者对丙酸屈他雄酮有反应,22%的患者对卵巢切除术有反应。在围绝经期组中,34.5%的患者对丙酸屈他雄酮有反应,39%的患者对苯丙酸诺龙有反应。在绝经后组中,57%的患者对雌激素有反应,38.5%的患者对丙酸屈他雄酮有反应。丙酸屈他雄酮的副作用一般不严重,很少有禁忌使用的情况。已证明丙酸屈他雄酮对所有年龄组都是一种有用且安全的制剂,尽管在绝经后患者中它似乎不如雌激素有效。