Velasco-Cornejo I F, Mion Júnior D, Martin L C, Tinucci T, Sampaio M, Pascoal I J, Athanázio-Heliodoro R C, Marcondes M, Franco R J
Faculdade de Medicina de Botucatu, UNESP, Faculdade de Medicina da USP.
Arq Bras Cardiol. 1994 Mar;62(3):159-64.
To evaluate the antihypertensive efficacy and safety of cilazapril compared to nifedipine retard in mild to moderate hypertension.
forty randomized out-patients with mild moderate hypertension, diastolic pressure (DP) between 95 and 115 mmHg, with placebo for 15 days were randomized and allocated for treatment, double-blind, once daily with cilazapril 2.5 mg (n = 20) or nifedipine retard 20 mg (20 = n) for four weeks. The non-responders (DP > 90mmHg) had the dosage increased twice, b.i.d., while responders were maintained up to 10 weeks. Clinical visits were performed before, at baseline and every two weeks and the laboratory test was performed after placebo run-in, 4th and 10th weeks of treatment.
The blood pressure (BP) were similar between groups at the end of the placebo (cilazapril 151 +/- 14/103 +/- 5 - nifedipine 157 +/- 17/108 +/- 7mmHg, p > 0.05). DP decreased already at second weeks (cilazapril 95 +/- 9 - nifedipine 96 +/- 11mmHg, p < 0.05, compared to week 0) in both groups at the end of study with no difference inter groups. BP normalization was obtained in 58% of the patients with cilazapril and in 61% in the nifedipine group. Adverse biochemical effects were not observed in any group. Six (16%) patients of the cilazapril and 15 (39%) of nifedipine related collateral events, although no difference were observed between groups.
Cilazapril 2.5 to 25mg normalized BP in 58% of mild and moderate hypertension patients, and this efficacy was similar to sustained-release nifedipine 20 to 40mg. Cilazapril had no adverse effects on the biochemical parameters with low incidence of collateral effects.
评估与缓释硝苯地平相比,西拉普利治疗轻至中度高血压的降压疗效及安全性。
40例轻中度高血压门诊患者,舒张压(DP)在95至115 mmHg之间,先服用15天安慰剂,之后随机分配接受双盲治疗,每日一次,服用西拉普利2.5 mg(n = 20)或缓释硝苯地平20 mg(n = 20),为期四周。无反应者(DP > 90 mmHg)剂量增加两次,每日两次,而有反应者持续治疗至10周。在治疗前、基线及每两周进行临床访视,并在安慰剂导入期后、治疗第4周和第10周进行实验室检查。
安慰剂期结束时,两组血压(BP)相似(西拉普利151 +/- 14/103 +/- 5 - 硝苯地平157 +/- 17/108 +/- 7 mmHg,p > 0.05)。研究结束时,两组在第二周DP均已下降(西拉普利95 +/- 9 - 硝苯地平96 +/- 11 mmHg,与第0周相比,p < 0.05),组间无差异。西拉普利组58%的患者和硝苯地平组61%的患者血压恢复正常。两组均未观察到不良生化效应。西拉普利组6例(16%)患者和硝苯地平组15例(39%)患者出现相关附带事件,尽管组间无差异。
2.5至25 mg西拉普利使58%的轻中度高血压患者血压恢复正常,该疗效与20至40 mg缓释硝苯地平相似。西拉普利对生化参数无不良影响,附带效应发生率低。