Efficacy of a low fixed-dose combination of penbutolol with piretanide in the treatment of mild to moderate hypertension: a double-blind study against placebo.

Pharmatherapeutica Pub Date : 1986-01-01
J Yasky, M Verho, B Rangoonwala
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Abstract

A double-blind crossover study was carried out in 20 patients with mild to moderate essential hypertension to assess the efficacy and tolerability of a low fixed-dose combination containing 20 mg penbutolol (a beta-blocking agent) and 3 mg piretanide (a diuretic) in comparison to placebo over a period of 4 weeks. Active drug treatment in the 20 patients studied was preceded by a 1-week period of placebo. The results showed that there was an effective significant reduction in systolic and diastolic blood pressure compared with initial levels in the fixed-dose combination group, when compared to the placebo group, both at rest, during maximal ergometric and isometric work load, and also in the diurnal blood pressure profile over 24 hours. Pulse rate also decreased in the combination group. The biochemical, haematological and urinary parameters showed no clinically relevant changes in either group during the entire study period. Minor side-effects definitely or probably associated with the treatment were observed in both groups but were generally mild and did not interfere with treatment. No patient withdrew prematurely from the trial.

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低固定剂量喷布托洛尔联合吡雷他尼治疗轻中度高血压的疗效:一项对照安慰剂的双盲研究。
一项双盲交叉研究对20名轻中度原发性高血压患者进行了为期4周的研究,以评估含有20mg戊布托洛尔(一种β阻断剂)和3mg吡脲(一种利尿剂)的低固定剂量组合与安慰剂的疗效和耐受性。在研究的20名患者中,积极药物治疗之前给予1周的安慰剂治疗。结果显示,与初始水平相比,固定剂量联合组的收缩压和舒张压有效显著降低,与安慰剂组相比,在休息时,在最大工效负荷和等距负荷期间,以及24小时内的日血压谱。联合用药组的脉搏率也有所下降。在整个研究期间,两组的生化、血液学和尿液参数均未出现临床相关的变化。在两组中都观察到轻微的副作用,这些副作用肯定或可能与治疗有关,但通常是轻微的,不会干扰治疗。没有患者过早退出试验。
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