首页> 外文期刊>JAMA: the Journal of the American Medical Association >Effect of galantamine hydrobromide in chronic fatigue syndrome: a randomized controlled trial.
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Effect of galantamine hydrobromide in chronic fatigue syndrome: a randomized controlled trial.

机译:加兰他敏氢溴酸盐在慢性疲劳综合征中的作用:一项随机对照试验。

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CONTEXT: There is no established pharmacological treatment for the core symptoms of chronic fatigue syndrome (CFS). Galantamine hydrobromide, an acetyl cholesterone inhibitor, has pharmacological properties that might benefit patients with CFS. OBJECTIVE: To compare the efficacy and tolerability of galantamine hydrobromide in patients with CFS. DESIGN, SETTING, AND PATIENTS: Randomized, double-blind trial conducted June 1997 through July 1999 at 35 outpatient centers in the United Kingdom (n = 17), United States (n = 14), the Netherlands (n = 2), Sweden (n = 1), and Belgium (n = 1) involving 434 patients with a clinical diagnosis of CFS (modified US Centers for Disease Control and Prevention criteria). INTERVENTIONS: A total of 89 patients were randomly assigned to receive 2.5 mg of galantamine hydrobromide; 86 patients, 5.0 mg; 91 patients, 7.5 mg; and 86 patients, 10 mg (these patients received medicine in the tablet form 3 times per day); a total of 82 patients received matching placebo tablets 3 times per day. MAIN OUTCOME MEASURES: The primary efficacy variable was the global change on the Clinician Global Impression Scale after 4, 8, 12, and 16 weeks of treatment. Secondary outcomes were changes in core symptoms of CFS on the Chalder Fatigue Rating Scale, the Fibromyalgia Impact Questionnaire, and the Pittsburgh Sleep Quality Index; changes in quality of life on the Nottingham Health Profile; and assessment of plasma-free cortisol levels and cognitive performance on a computer-based battery of tests. RESULTS: After 16 weeks, there were no statistically significant differences between any of the galantamine or placebo groups in clinical condition on the Clinician Global Impression Scale, or for any of the secondary end points. Exploratory regression analysis failed to detect any consistent prognostic factor that might have influenced the primary or any secondary outcome measures. CONCLUSION: This trial did not demonstrate any benefit of galantamine over placebo in the treatment of patients with CFS.
机译:背景:目前尚无针对慢性疲劳综合征(CFS)核心症状的药物治疗方法。加兰他敏氢溴酸盐是一种乙酰胆甾酮抑制剂,其药理特性可能会使CFS患者受益。目的:比较加兰他敏氢溴酸盐对CFS的疗效和耐受性。设计,地点和患者:1997年6月至1999年7月在英国(n = 17),美国(n = 14),荷兰(n = 2),瑞典的35个门诊中心进行的随机双盲试验(n = 1),比利时(n = 1)涉及434例临床诊断为CFS的患者(美国疾病控制和预防中心标准修订版)。干预措施:共有89名患者被随机分配接受2.5 mg加兰他敏氢溴酸盐治疗; 86名患者,5.0毫克; 91例患者,7.5 mg; 86例患者,剂量为10 mg(这些患者每天服用3片药片);共有82例患者每天接受3次匹配的安慰剂片剂。主要观察指标:主要疗效变量是治疗4、8、12和16周后临床医生总体印象量表的总体变化。次要结果是Chalder疲劳评分量表,纤维肌痛影响问卷和匹兹堡睡眠质量指数对CFS核心症状的改变。诺丁汉健康概况上的生活质量变化;在基于计算机的一系列测试中评估和评估无血浆皮质醇水平和认知能力。结果:16周后,在临床情况上,根据临床医生全球印象量表或任何次要终点,加兰他敏或安慰剂组之间在统计学上无显着差异。探索性回归分析未能发现任何可能影响主要或次要结局指标的一致预后因素。结论:该试验并未证明加兰他敏在安慰剂治疗中比安慰剂有任何益处。

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