哌醋甲酯
安慰剂
癌症相关疲劳
医学
安慰剂组
临床试验
内科学
麻醉
癌症
精神科
注意缺陷多动障碍
病理
替代医学
作者
Carlos Centeno,Rocio Rojí,María Angustias Portela,Ana de Santiago,Miguel Ángel Cuervo,Daniel Ramos,Á. F. Gândara,Esteban Salgado,Bruno Gagnon,Álvaro Sanz Rubiales
出处
期刊:BMJ supportive & palliative care
[BMJ]
日期:2020-11-09
卷期号:12 (2): 226-234
被引量:18
标识
DOI:10.1136/bmjspcare-2020-002454
摘要
Methylphenidate is a psychostimulant drug used to treat fatigue in patients with advanced cancer, for which there is no gold standard of treatment.To explore the efficacy of methylphenidate in the relief of fatigue in patients with advanced cancer.A randomised double-blind placebo-controlled multicentre clinical trial, stratified according to the intensity of fatigue. The treatment was considered effective if the improvement in mean fatigue intensity between baseline values and day 6 was significantly higher in the methylphenidate group than in the placebo group. The responses were measured using the Edmonton Symptoms Assessment System (ESAS) and the Functional Assessment of Cancer Therapy-Fatigue (FACT-F) scales.35 patients received placebo and 42 patients received methylphenidate. The populations of both groups were homogeneous. Patients receiving methylphenidate did not exhibit statistically significant improvement of fatigue in comparison to patients receiving placebo (p=0.52). The mean improvement of fatigue (ESAS) on day 6 was -1.9 (±2.5) in the placebo group, and -2.3 (±2.6) in the methylphenidate group (p=0.52). The results obtained with the FACT-F were congruent with those obtained by the ESAS. The responses in patients with severe fatigue were -2.4 (±2.9) in the placebo group and -3.4 (±2.5) in the methylphenidate group; the difference was not statistically significant (p=0.3).Methylphenidate was not more efficient than placebo to treat cancer-related fatigue. Fatigue improved significantly after 3 days of treatment and was stabilised on day 6, both with placebo and methylphenidate. The side effects of methylphenidate were mild and infrequent.EudraCT Registry (2008-002171-27).
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