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临床试验/NCT04419272
NCT04419272
招募中
4 期

Methylphenidate for the Treatment of Epilepsy-related Cognitive Deficits: a Randomized, Double-blind, Placebo-controlled Trial

VA Office of Research and Development8 个研究点 分布在 1 个国家目标入组 226 人2023年8月14日
适应症Epilepsy
相关药物Methylphenidate

概览

阶段
4 期
干预措施
Placebo
疾病 / 适应症
Epilepsy
发起方
VA Office of Research and Development
入组人数
226
试验地点
8
主要终点
Change in Conners Continuous Performance Test (CPT), Following Placebo vs. Methylphenidate
状态
招募中
最后更新
12天前

概览

简要总结

Methylphenidate (MPH) is a stimulant, FDA-approved for the treatment of attention deficit hyperactivity disorder (ADHD). It is unknown, however, if stimulants would be of benefit for memory and thinking problems due to epilepsy. In this study, participants will be assigned randomly (i.e., by flip of a coin), to a group that takes MPH and a group that takes a placebo (sugar pill). Participants will not know the group to which they have been assigned. Tests of attention and memory will be completed before taking the study pills and at Week 8. All participants will then have the option of taking MPH for the next two months, and attention and memory will be tested again at Week 16. The study will determine whether methylphenidate is helpful for the treatment of attention and memory problems in adults with epilepsy, and whether the medication is safe and beneficial when taken over an extended time period.

详细描述

The proposed study is a randomized, double-blind trial of MPH vs. placebo in subjects with epilepsy and impaired attention. In the blinded phase, subjects will receive placebo or MPH (titrated to 20mg twice daily) for 8 weeks. Subjects will then receive open-label MPH for 8 weeks (titrated to 20mg twice daily). Cognitive tests will be performed at baseline, Week 8 (the end of the double-blind period), and at Week 16 (the end of the open-label period). The primary aim is to evaluate the efficacy of MPH for the treatment of attentional dysfunction in subjects with epilepsy. It is expected that subjects will have improved attention when taking MPH compared to placebo, measured by the Conner's Continuous Performance Test (CPT). The effects of MPH on other cognitive functions that rely in part on attention, including a composite measure of memory (MCG Paragraph Test), psychomotor speed (Symbol Digit Modalities Test), and divided attention, psychomotor speed, and response inhibition (Stroop Color Word Interference Test), will be ascertained. Improved performance when taking MPH compared to placebo is expected. Finally, the study will establish the effect of MPH on overall quality of life. It is hypothesized that there will be improvement in self-reported quality of life with MPH, but no change with placebo, as assessed by the Quality of Life in Epilepsy Patient Inventory. We will evaluate the safety of MPH compared to placebo with respect to seizure frequency. Secondary analyses will determine continued efficacy over an open-label period. To control for practice effects, cognitive performance will be compared to healthy subjects and epilepsy patients without cognitive complaints, who will complete the repeated cognitive measures but remain untreated for the duration of the trial.

注册库
clinicaltrials.gov
开始日期
2023年8月14日
结束日期
2028年5月31日
最后更新
12天前
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

责任方
Sponsor

入排标准

入选标准

  • SUBJECTS WITH EPILEPSY
  • Participants will include adult subjects with focal-onset epilepsy, based on clinical history, imaging studies and ictal and/or interictal EEG interpreted by a clinical epileptologist. Seizures may be symptomatic, idiopathic, traumatic, or non- traumatic in etiology. Subjects must have self-reported cognitive dysfunction. Subjects must also meet the following eligibility criteria:
  • Age 18 years of age or older;
  • Capacity to provide informed consent;
  • Ability to live independently and complete activities of daily living;
  • Stable seizure frequency at the time of enrollment, such that the subject's treating physician does not believe a change in ASM regimen to be warranted during the trial (ASMs should remain unchanged during the 16 weeks of participation unless absolutely required clinically due an unanticipated change in seizure frequency or severity);
  • Fluency in written and spoken English.
  • CONTROLS \*DO NOT UNDERGO ANY DRUG OR PLACEBO INTERVENTION Two additional subject groups will be included, to control for effects of repeated testing in the open-label extension phase: healthy subjects and epilepsy patients without cognitive complaints, who will not receive the study drug at any point during the study. Epilepsy patients without cognitive deficits must otherwise meet all of the above criteria.
  • Healthy controls must meet the following inclusion criteria:
  • Age 18 years or older;

排除标准

  • SUBJECTS WITH EPILEPSY
  • Subjects with epilepsy with or without cognitive complaints will be excluded from participation for:
  • Psychogenic, non-epileptic spells
  • Delirium in the past year
  • Other progressive neurologic illness (i.e., malignant brain tumor). A benign, stable neoplasm with no plans for resection will not be cause for exclusion.
  • A history of alcohol or illicit drug abuse;
  • Generalized tonic-clonic or other generalized motor seizure(s) within 48 hours or focal-onset seizures with impaired awareness within 24 hours of neuropsychological testing;
  • Status epilepticus in the past year;
  • Neurosurgery within the past 6 months;
  • Active suicidal plan/intent in the past 6 months, a history of suicide attempt in the last 2 years, more than 1 lifetime suicide attempt, and/or current high-risk suicide flag in the medical record;

研究组 & 干预措施

Placebo

Subjects who will receive placebo in the double-blinded period; when assigned to receive the placebo during the double-blinded period, subjects will be given a sugar pill for 8 weeks. The sugar pill will be taken twice per day, at 8am and 12pm.

干预措施: Placebo

Open-Label Methylphenidate

All subjects will be offered open-label methylphenidate during Weeks 9-16. the dosage of MPH will begin at 10mg twice per day, at 8am and 12pm, for one week. The dosage will then increase to 20mg twice daily, at 8am and 12pm, for the next 7 weeks.

干预措施: Methylphenidate

Methylphenidate

Subjects who will receive methylphenidate in the double-blinded period; when assigned to the active drug, the dosage of MPH will begin at 10mg twice per day, at 8am and 12pm, for one week. The dosage will then increase to 20mg twice daily, at 8am and 12pm, for the next 7 weeks.

干预措施: Methylphenidate

结局指标

主要结局

Change in Conners Continuous Performance Test (CPT), Following Placebo vs. Methylphenidate

时间窗: Week 8

Conners Continuous Performance Test (CPT) d' value, a measure of attention, compared post-placebo vs. post-methylphenidate (MPH) in a double-blind, parallel group, placebo controlled, randomized design

次要结局

  • Change in Composite Measure of Cognition, Following Placebo vs. Methylphenidate(Week 8)
  • Change in Overall Quality of Life, Following Placebo vs. Methylphenidate(Week 8)
  • Change in Composite Measure of Cognition, Post-Open-Label(Week 16)
  • Change in Subjective Cognitive Function, Following Placebo vs. Methylphenidate(Week 8)
  • Change in Subjective Cognitive Function, Post-Open-Label(Week 16)
  • Change in Overall Subjective Quality of Life, Post-Open-Label(Week 16)
  • Effects on Seizure Frequency(Week 8, Week 16)
  • Change in Conner's Continuous Performance Test (CPT), Post-Open-Label(Week 16)
  • Visual Paired Comparison Task Novelty Preference Score Following Placebo vs. Methylphenidate(Week 8)
  • Change in Conners Continuous Performance Test (CPT), Comparing Methylphenidate Group to Untreated Controls(Week 8, Week 16)
  • Change in Digit Span Following Placebo vs. Methylphenidate(Week 8)
  • Change in Digit Span, Post-Open-Label(Week 16)

研究点 (8)

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