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作 者:赵秀丽[1] 周延明[2] 李洁[1] 肖洁[1] 王建旗[1] 周辉[1]
机构地区:[1]首都医科大学附属北京同仁医院,北京100730 [2]黑龙江省公安厅安康医院,哈尔滨150078
出 处:《中国新药杂志》2008年第2期157-160,共4页Chinese Journal of New Drugs
摘 要:目的:评价西尼地平治疗轻中度原发性高血压的有效性和安全性。方法:采用随机对照、双盲双模拟研究设计。48例患者分为试验组和对照组各24例。试验组患者口服西尼地平片和苯磺酸氨氯地平模拟片,西尼地平起始剂量为5 mg,qd,4周后若舒张压≥90 mmHg,则增加至10 mg,qd,直至试验结束。对照组口服苯磺酸氨氯地平片和西尼地平模拟片,给药方法及剂量调整与试验组相同。结果:8周后试验组和对照组的收缩压降低幅度分别为(11.13±7.31)和(16.10±7.68)mmHg,最大舒张压降低幅度分别为(11.01±4.17)和(13.27±4.57)mmHg,治疗前后组内比较均有统计学意义。8周末两组间收缩压降低幅度有显著差异(P<0.05)。两组均无严重不良反应发生,每组各有5例发生药物不良反应,无统计学差异(P>0.05)。结论:西尼地平每日服用1次降压安全有效。Objective: To investigate the efficacy and safety of cilnidipine in the treatment of mild to moderate essential hypertension. Methods: The study design was randomized, controlled, double blind and double simulated. One half of 48 patients (n = 24) were orally given cilnidipine and amlodipine besylate mimesis tablet. The initial dose of cilnidipine was 5 mg per day; after 4 weeks, the dose was increased to 10 mg per day until the end of the study if the diastolic blood pressure was equal or above 90 mmHg. Other patients (n = 24) were orally given amlodipine besylate and cilnidipine mimesis tablet in the same administration and doses. Results : At 8 weeks after treatment, systolic blood pressure was decreased by ( 11. 13± 7.31 ) mmHg and ( 16. 10 ± 7.68 ) mmHg in cilnidipine and amlodipine groups (P 〈 0. 05 ), respectively. The diastolic blood pressure was decreased by ( 11.01 ± 4.17 ) mmHg and ( 13.27± 4.57 ) mmHg in cilnidipine and amlodipine group, respectively. There were significant differences in systolic and diastolic blood pressure before and after both treatments. No serious adverse reaction occurred after 2 treatments; however, the adverse reaction occurred in 5 patients in either cilnidipine or amlodipine group (P 〉 0.05) , respectively. Conclusion: Oral cilnidipine once daily is effective and safe in the treatment of mild to moderate essential hypertension.
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