Frederick Vinckenbosch, Gert Jan Lammers, Sebastiaan Overeem, Dan Chen, Grace Wang, Lawrence P. Carter, Kefei Zhou, Johannes G. Ramaekers, Annemiek Vermeeren
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The primary endpoint was standard deviation of lateral position (SDLP) at 2 h post-dose.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>The study included 24 participants (54% male; mean age, 40 years); 22 had evaluable SDLP data. At 2 h post-dose, median SDLP was significantly lower (improved) with solriamfetol compared with placebo (19.08 vs. 20.46 cm [median difference, −1.9 cm], <i>p</i> = 0.002). Four participants on solriamfetol and 7 on placebo had incomplete driving tests. At 6 h post-dose, median SDLP was not statistically significantly different with solriamfetol compared with placebo (19.59 vs. 19.78 cm [median difference, −1.1 cm], <i>p</i> = 0.125). Three participants on solriamfetol and 10 on placebo had incomplete driving tests. 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引用次数: 2
摘要
目的探讨多巴胺和去甲肾上腺素再摄取抑制剂索利氨酚对嗜睡患者道路驾驶行为的影响。在这项随机、双盲、安慰剂对照的交叉研究中,研究人员在索利氨酚(150 mg/天,连续3天,随后300 mg/天,连续4天)或安慰剂治疗7天后的第2和6小时,对1小时道路驾驶测试中的驾驶表现进行了评估。主要终点是给药后2小时的侧位标准偏差(SDLP)。结果共纳入24例受试者,其中男性占54%;平均年龄40岁);22例有可评价的SDLP数据。在给药后2小时,与安慰剂相比,索利氨酚的中位SDLP显著降低(改善)(19.08 vs 20.46 cm[中位差,−1.9 cm], p = 0.002)。4名服用索利氨酚的参与者和7名服用安慰剂的参与者驾驶测试不完整。在给药后6小时,索利氨酚与安慰剂相比,中位SDLP无统计学差异(19.59 vs 19.78 cm[中位差,- 1.1 cm], p = 0.125)。服用索利氨酚的3名参与者和服用安慰剂的10名参与者驾驶测试不完整。常见的不良事件(≥5%)包括头痛、食欲下降和嗜睡。结论索利安非托尔300 mg/天改善了发作性睡症患者服药后2小时的道路驾驶表现。
Effects of solriamfetol on on-the-road driving in participants with narcolepsy: A randomised crossover trial
Objective
To evaluate the impact of solriamfetol, a dopamine and norepinephrine reuptake inhibitor, on on-the-road driving performance in participants with narcolepsy.
Methods
In this randomised, double-blind, placebo-controlled, crossover study, driving performance during a 1 h on-road driving test was assessed at 2 and 6 h post-dose following 7 days of treatment with solriamfetol (150 mg/day for 3 days, followed by 300 mg/day for 4 days) or placebo. The primary endpoint was standard deviation of lateral position (SDLP) at 2 h post-dose.
Results
The study included 24 participants (54% male; mean age, 40 years); 22 had evaluable SDLP data. At 2 h post-dose, median SDLP was significantly lower (improved) with solriamfetol compared with placebo (19.08 vs. 20.46 cm [median difference, −1.9 cm], p = 0.002). Four participants on solriamfetol and 7 on placebo had incomplete driving tests. At 6 h post-dose, median SDLP was not statistically significantly different with solriamfetol compared with placebo (19.59 vs. 19.78 cm [median difference, −1.1 cm], p = 0.125). Three participants on solriamfetol and 10 on placebo had incomplete driving tests. Common adverse events (≥5%) included headache, decreased appetite, and somnolence.
Conclusions
Solriamfetol 300 mg/day improved on-the-road driving performance, at 2 h post-administration in participants with narcolepsy.
期刊介绍:
Human Psychopharmacology: Clinical and Experimental provides a forum for the evaluation of clinical and experimental research on both new and established psychotropic medicines. Experimental studies of other centrally active drugs, including herbal products, in clinical, social and psychological contexts, as well as clinical/scientific papers on drugs of abuse and drug dependency will also be considered. While the primary purpose of the Journal is to publish the results of clinical research, the results of animal studies relevant to human psychopharmacology are welcome. The following topics are of special interest to the editors and readers of the Journal:
-All aspects of clinical psychopharmacology-
Efficacy and safety studies of novel and standard psychotropic drugs-
Studies of the adverse effects of psychotropic drugs-
Effects of psychotropic drugs on normal physiological processes-
Geriatric and paediatric psychopharmacology-
Ethical and psychosocial aspects of drug use and misuse-
Psychopharmacological aspects of sleep and chronobiology-
Neuroimaging and psychoactive drugs-
Phytopharmacology and psychoactive substances-
Drug treatment of neurological disorders-
Mechanisms of action of psychotropic drugs-
Ethnopsychopharmacology-
Pharmacogenetic aspects of mental illness and drug response-
Psychometrics: psychopharmacological methods and experimental design