Efficacy of penbutolol and a combination of a low dose of penbutolol with piretanide in the treatment of mild to moderate hypertension.

Pharmatherapeutica Pub Date : 1985-01-01
E Graml, M Verho, B Rangoonwala, R Englert, E Häringer, K Pahnke
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Abstract

A double-blind study was carried out in two parallel groups of patients with mild to moderate hypertension to assess the efficacy and tolerance of the combination 20 mg penbutolol plus 3 mg piretanide in comparison to 40 mg penbutolol alone over a period of 6 weeks. Active drug treatment in the 51 patients studied was preceded by a 2-week period of placebo. The results showed that in both groups there was an effective reduction in systolic and diastolic blood pressure compared with initial levels. Although there was no significant difference between the groups, the normalization of diastolic blood pressure (less than 95 mmHg) was achieved in 70% of the patients receiving the combination and in 59% of the patients treated with penbutolol alone. Pulse rate decreased in both groups, body weight only in the combination group. The biochemical and haematological parameters showed no clinically relevant changes during treatment with either drug regimens. 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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喷布托尔与小剂量喷布托尔联合吡雷他尼治疗轻中度高血压的疗效观察。
在两组轻度至中度高血压患者中进行了一项双盲研究,以评估20mg喷布托尔加3mg吡雷他尼与40mg喷布托尔单独联合使用的疗效和耐受性,为期6周。在研究的51名患者中,积极的药物治疗之前有2周的安慰剂期。结果显示,与初始水平相比,两组患者的收缩压和舒张压均有效降低。虽然两组之间没有显著差异,但70%的联合用药患者和59%的单用喷布托洛尔患者的舒张压达到了正常化(低于95 mmHg)。两组脉搏率均下降,仅联合用药组体重下降。两种药物治疗期间生化和血液学参数均无临床相关变化。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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