首页> 外文期刊>Pilot and Feasibility Studies >A protocol for a randomised controlled, double-blind feasibility trial investigating fluoxetine treatment in improving memory and learning impairments in patients with mesial temporal lobe epilepsy: Fluoxetine, Learning and Memory in Epilepsy (FLAME trial)
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A protocol for a randomised controlled, double-blind feasibility trial investigating fluoxetine treatment in improving memory and learning impairments in patients with mesial temporal lobe epilepsy: Fluoxetine, Learning and Memory in Epilepsy (FLAME trial)

机译:一项关于氟西汀治疗改善中颞叶癫痫患者记忆和学习障碍的随机对照,双盲可行性试验的方案:氟西汀,癫痫的学习和记忆(FLAME试验)

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BackgroundPeople with temporal lobe epilepsy (TLE) report significant problems with learning and memory. There are no effective therapies for combatting these problems in people with TLE, resulting in an unmet therapeutic need. The lack of treatment is, in part, due to a poor understanding of the neurobiology underlying these memory deficits. We know that hippocampal neurogenesis, a process believed to be important in learning and memory formation, is permanently reduced in chronic TLE, and this may go some way to explain the learning and memory impairments seen in people with TLE.The common anti-depressant drug fluoxetine has been shown to stimulate neurogenesis both in the healthy brain and in neurological diseases where neurogenesis is impaired. In an animal model of TLE, administration of fluoxetine was found to restore neurogenesis and improve learning on a complex spatial navigational task. We now want to test this effect in humans by investigating whether administration of fluoxetine to people with TLE can improve learning and memory.MethodsThis is a single-centre randomised controlled, double-blind feasibility trial. We plan to recruit 20 participants with a diagnosis of TLE and uni-lateral hippocampal sclerosis, confirmed by 3T MRI. Eligible participants will undergo baseline assessments of learning and memory prior to being randomised to either 20 mg/day fluoxetine or matching placebo for 60 days. Follow-up assessments will be conducted after 60 days of trial medication and then again at 60 days after cessation of trial medication. Feasibility will be assessed on measures of recruitment, retention and adherence against pre-determined criteria.DiscussionThis trial is designed to determine the feasibility of conducting a double-blind randomised controlled trial of fluoxetine for the treatment of learning and memory impairments in people with TLE. Data collected in this trial will inform the design and utility of any future efficacy trial involving fluoxetine for the treatment of learning and memory in people with TLE.
机译:背景颞叶癫痫(TLE)的人们报告了学习和记忆方面的重大问题。目前尚无有效的疗法可解决TLE患者的这些问题,从而导致治疗需求未得到满足。缺乏治疗的部分原因是对这些记忆缺陷背后的神经生物学了解不足。我们知道,慢性TLE永久性减少了海马神经发生,这一过程被认为对学习和记忆形成很重要,这可能有助于解释TLE患者的学习和记忆障碍。常见的抗抑郁药氟西汀已被证明可在健康的大脑和神经发生受损的神经系统疾病中刺激神经发生。在TLE的动物模型中,发现氟西汀的给药可恢复神经发生并改善复杂空间导航任务的学习。我们现在想通过研究对TLE患者使用氟西汀是否可以改善学习和记忆能力来在人类中测试这种效果。方法这是一项单中心随机对照,双盲可行性试验。我们计划招募20名经TLE和单侧海马硬化诊断为3T MRI证实的参与者。符合条件的参与者将接受学习和记忆的基线评估,然后随机分配给20毫克/天的氟西汀或匹配的安慰剂60天。在试用药物治疗60天后进行随访评估,然后在终止试用药物治疗60天后再次进行评估。将根据预先确定的标准评估招募,保留和坚持的措施的可行性。讨论该试验旨在确定进行氟西汀双盲随机对照试验以治疗TLE患者的学习和记忆障碍的可行性。该试验收集的数据将为将来涉及氟西汀治疗TLE患者的学习和记忆的任何功效试验提供设计和实用性。

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