Indian J Med Res. 1998 Jul;108:24-9.
A flexible dose open trial was undertaken in four centres in India to evaluate the efficacy of an Ayurvedic drug Vijayasar (Pterocarpus marsupium) in the treatment of newly-diagnosed or untreated non-insulin dependent diabetes mellitus (NIDDM). By 12 wk, control of blood glucose (both fasting and postprandial levels) had been attained in 67 (69%) of 97 patients studied, and the dose on which control was attained was 2 g of the extract in about 73 per cent of the patients, 3 g in about 16 per cent and 4 g in 10 per cent of the patients. Four patients had to be withdrawn from treatment due to excessively high postprandial blood glucose levels. Among the 93 patients who completed 12 wk of treatment, both the fasting and postprandial blood glucose levels fell significantly (P < 0.001), by 32 and 45 mg/dl at 12 wk from the initial means of 151 and 216 mg/dl respectively. Mean HbA1c decreased significantly (P < 0.001) to 9.4 per cent at 12 wk from the initial mean of 9.8 per cent. No significant change was observed in the mean levels of lipids. Other laboratory parameters remained stable during the designated treatment period of 12 wk. Also, no side-effects were reported. Hence, it is concluded that Vijayasar is useful in the treatment of newly diagnosed or untreated mild NIDDM patients.
在印度的四个中心进行了一项灵活剂量的开放试验,以评估一种阿育吠陀药物维贾亚萨尔(阔叶紫檀)治疗新诊断或未经治疗的非胰岛素依赖型糖尿病(NIDDM)的疗效。到12周时,在研究的97例患者中,有67例(69%)实现了血糖控制(空腹和餐后水平),实现血糖控制的剂量在约73%的患者中为2克提取物,约16%的患者为3克,10%的患者为4克。4例患者因餐后血糖水平过高而不得不退出治疗。在完成12周治疗的93例患者中,空腹和餐后血糖水平均显著下降(P<0.001),12周时分别从初始均值151和216毫克/分升降至32和45毫克/分升。平均糖化血红蛋白(HbA1c)从初始均值9.8%显著下降(P<0.001)至12周时的9.4%。血脂均值未观察到显著变化。在指定的12周治疗期间,其他实验室参数保持稳定。此外,未报告有副作用。因此,得出结论,维贾亚萨尔对新诊断或未经治疗的轻度NIDDM患者的治疗有用。