Zuclopenthixol and melperon in the treatment of elderly patients: a double-blind, controlled, multi-centre study.

Pharmatherapeutica Pub Date : 1988-01-01
H Nygaard, K Bakke, E Brudvik, G K Lien, T J Moe, K Elgen
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Abstract

A double-blind study was carried out in 53 elderly patients in 6 geriatric nursing homes to assess the effectiveness of the neuroleptics, zuclopenthixol and melperon (flubuperone), in the relief of restlessness, aggressiveness and other such symptoms. The initial daily dose was 4 mg zuclopenthixol or 75 mg melperon, increased if necessary over the treatment period of 4 weeks. Assessments were made on entry and after 1, 2 and 4 weeks of treatment of the overall severity of illness and of individual symptoms. The results showed that there was significant improvement in the condition of patients in both treatment groups and a significant reduction in mean total as well as in the main single symptom scores. These changes were already apparent after 1 week of treatment. Although there was a tendency for faster improvement in the zuclopenthixol group, there were no significant differences between the groups in any of the parameters assessed. Side-effects were few and generally mild and transient.

Zuclopenthixol和melperon治疗老年患者:一项双盲、对照、多中心研究。
采用双盲方法对6家老年护理机构的53例老年患者进行研究,评估抗精神病药zuclopenthixol和melperon(氟布酮)对烦躁不安、攻击性等症状的缓解效果。初始每日剂量为4毫克zuclopenthixol或75毫克melperon,在4周的治疗期间如有必要可增加剂量。在入组时以及治疗1、2和4周后,对疾病的总体严重程度和个别症状进行评估。结果显示,两组患者的病情均有显著改善,平均总评分和主要单一症状评分均有显著降低。这些变化在治疗1周后已经很明显。虽然zuclopenthxol组有更快改善的趋势,但在评估的任何参数中,两组之间没有显着差异。副作用很少,通常是轻微和短暂的。
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