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克拉霉素在嗜睡综合征中的作用机制

2026年7月16日 更新者:Lynn Marie Trotti、Emory University

抗生素介导的警惕性改善:克拉霉素在嗜睡综合征中的作用机制

本研究的目的是评估一种名为克拉霉素的药物在两种相关情况下治疗嗜睡的效果,即不伴猝倒的发作性睡病和特发性嗜睡症。 研究表明,克拉霉素可以减少嗜睡,但研究人员不知道克拉霉素是如何做到这一点的。 这项研究将着眼于大脑活动(磁共振成像 [MRI] 和脑电图 [EEG] 脑电波)、炎症、肠道细菌和脑脊液,以更好地了解克拉霉素如何减少嗜睡。 这项研究将招募 92 名参与者,他们将被随机分配接受为期 14 天的克拉霉素或安慰剂。

研究概览

详细说明

白天过度嗜睡和睡眠持续时间长是许多神经系统疾病的共同特征,包括强直性肌营养不良、帕金森病和中枢神经系统嗜睡综合征。 后一种综合征是一组具有重叠临床表型的疾病,并且除了由于伪君子缺乏症(发作性睡病 1 型)引起的发作性睡病外,可能具有共同的病理生理学。

这些疾病的病态白天嗜睡会损害职业表现,限制生活质量,并使机动车和其他事故风险增加一倍以上。 由于大多数这些嗜睡综合征的根本原因尚不清楚,因此治疗旨在增加参与觉醒促进的单胺能信号。 然而,至少有四分之一的嗜睡症患者无法通过这些治疗达到令人满意的症状控制,因此通常需要残疾或病假。 显然需要针对白天过度嗜睡的新疗法来解决当前护理标准的失败。

在之前的研究中,克拉霉素可显着改善嗜睡严重程度、与嗜睡相关的日常活动扩展限制以及与嗜睡相关的生活质量。 克拉霉素也改善了睡眠持续时间长和睡眠惯性这两种导致功能障碍的嗜睡症的辅助症状。

假设:根据自我报告和客观测试的衡量,克拉霉素将减少过度嗜睡和嗜睡症的其他症状。

目的 1:确定克拉霉素在中枢性嗜睡综合征患者中促进觉醒和减少嗜睡能力的中枢神经系统介质。

假设 1a:体外脑脊液 (CSF) γ-氨基丁酸-A (GABA-A) 受体功能增强的变化与自我报告和客观测量的嗜睡的改善有关。

假设 1b:功能连接的变化将与自我报告和客观测量的嗜睡的改善有关。

目标 2:探讨克拉霉素可能减少中枢性嗜睡综合征患者嗜睡的神经元外机制,包括全身炎症的变化和胃肠道微生物群组成的变化。

假设 2a:使用克拉霉素改善嗜睡与全身炎症的减少呈正相关,尤其是肿瘤坏死因子-α (TNFα) 水平的降低。

假设 2b:使用克拉霉素改善嗜睡与胃肠道生态失调的调节呈正相关。

研究类型

介入性

注册 (实际的)

83

阶段

  • 阶段2

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • Georgia
      • Atlanta、Georgia、美国、30329
        • Emory Sleep Center

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 60年 (成人)

接受健康志愿者

不

描述

纳入标准:

  • 特发性嗜睡症或发作性睡病 2 型的诊断
  • 18-60岁
  • 没有服用促醒药物,尽管目前服用促醒药物仍困倦,或愿意在基线测量前停止目前的促醒药物至少 5 个半衰期
  • 在基线测量前至少六个月不服用益生菌或益生菌补充剂

排除标准:

  • 嗜睡的其他潜在原因,包括中度或重度睡眠呼吸暂停、伴觉醒的严重周期性肢体运动障碍、不受控制的代谢紊乱、伪君子缺乏症或猝倒症
  • 克拉霉素禁忌症
  • 任何研究程序的禁忌症

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:基础科学
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的:克拉霉素
该研究组的参与者将接受为期 14 天的克拉霉素治疗。
克拉霉素的剂量为 500 毫克,每天两次,一次在醒来时,一次在午餐时服用,持续 14 天。
其他名称:
  • 比心
安慰剂比较:安慰剂
该研究组的参与者将接受安慰剂以匹配克拉霉素 14 天。
与克拉霉素相匹配的安慰剂剂量为 500 毫克,每天两次,一次在醒来时,一次在午餐时服用,持续 14 天。

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in Epworth Sleepiness Scale (ESS) Score
大体时间:Day -1, Day 14
The Epworth Sleepiness Scale asks participants to respond to 8 scenarios with how likely they are to fall asleep on a 4-point scale where 0 = "would never doze" and 3 = "high chance of dozing". Total scores range from 0 to 24 where higher scores indicate a higher chance of falling asleep during daytime activities. The change in ESS score is obtained by subtracting the total score at Day 14 from the baseline score. Scores above 0 mean that the mean score at Day 14 was lower than the mean score at Baseline, indicating less sleepiness.
Day -1, Day 14
Change in Maintenance of Wakefulness Test (MWT) for Sleep Latency
大体时间:Day -1, Day 14
The MWT polysomnographic procedure for sleep latency examines how well participants stay awake during several trials where participants relax in a quiet room for 40 minutes. One study found the mean sleep latency among persons without a sleep disorder to be 35.2 minutes. The change from baseline is calculated as baseline sleep latency minus sleep latency at Day 14, in minutes. Positive values result when the duration of sleep latency at Day 14 is lower than at Baseline.
Day -1, Day 14
Change in Gamma-aminobutyric Acid Receptor A (GABA-A) Potentiation
大体时间:Day -1, Day 14
Cerebrospinal fluid (CSF) is drawn to determine the change in levels of GABA-A potentiation between the study arms. The difference between measured current with GABA alone and the current measured with GABA + CSF yields a measure of potentiation for each CSF sample in each condition. The change from baseline is calculated as the baseline value minus the value at Day 14.
Day -1, Day 14
Change in Default Mode Network (DMN) Connectivity
大体时间:Day -2, Day 13
The default mode network (DMN) consists of a group of highly correlated brain regions most active during quiet rest, while the task positive network (TPN) is the brain network activated for goal-directed tasks. DMN connectivity changes with sleep states and it is increasingly implicated in the symptomatology of sleepiness. During resting state, sleep deprived participants demonstrate reduced static connectivity with the DMN. Changes in DMN between the Baseline 1 (Day - 2) and Day 13 visits are compared between treatment groups, particularly using quasi-periodic patterns (QPPs), which interrogate network-level connectivity on a dynamic scale. Preservation of the temporal dimension provides more insight into how this spatiotemporal network propagates across condition and pathology. The DMN/TPN QPP correlation is reported.
Day -2, Day 13
Change in Tumor Necrosis Factor - Alpha (TNF-α)
大体时间:Day -1, Day 14
Blood samples are used to determine the change in levels of TNF-α between the study arms. TNF-α is a soporific cytokine and a reduction in soporific cytokines is hypothesized to reduce daytime sleepiness.
Day -1, Day 14
Change in Gastrointestinal Microbiome Composition
大体时间:Day -1, Day 14
Changes in microbiome composition, as measured by alpha diversity using the Shannon Index, via 16S ribosomal ribonucleic acid (rRNA) sequencing results are compared between study arms. The Shannon Index measures both abundance and evenness of microbial species, values of 0 indicate that a community has only one species. The higher the value the higher the diversity of species in a particular community. Change from baseline is calculated by subtracting the Day 14 value from the value at Baseline. Numbers greater than 0 indicate that the Day 14 Shannon index value is lower than at Baseline.
Day -1, Day 14

次要结果测量

结果测量
措施说明
大体时间
On-Treatment Sleep Duration
大体时间:Day 1 through Day 14
Participants log when they go to bed and when they wake up in order to calculate the number of minutes spent sleeping. The average duration of sleep across 14 days is compared between study arms.
Day 1 through Day 14
Change in Fatigue Severity Scale (FSS) Score
大体时间:Day -1, Day 14
Fatigue severity is measured with the Fatigue Severity Scale (FSS). The FSS is a 9-item instrument where responses are on a scale of 1 to 7 where 1 = "disagree" and 7 = "agree". Total scores range from 9 to 63 where higher scores indicate greater fatigue. The change in FSS score is obtained by subtracting the total score at Day 14 from the Baseline score. Scores above 0 signify that the mean score at Day 14 was lower than the mean score at Baseline, indicating decreased fatigue.
Day -1, Day 14
Change in Multidimensional Fatigue Inventory (MFI-20) Score
大体时间:Day -1, Day 14
The MFI-20 is a 20-item instrument assessing fatigue severity. Responses are on a 5-point scale where 1 = "yes, that is true" and 5 = "no, that is not true". Positively phrased items are reverse scored so that the total score ranges from 20 to 100 where higher scores indicate greater severity of fatigue. The change in MFI-20 score is obtained by subtracting the total score at Day 14 from the Baseline score. Scores above 0 signify that the mean score at Day 14 was lower than the mean score at Baseline, indicating decreased fatigue.
Day -1, Day 14
Change in Sleep Inertia Questionnaire (SIQ) Score
大体时间:Day -1, Day 14
The SIQ is an instrument with 21 items with responses on a 5-point scale where 1 = "not at all" and 5 = "all the time". Two additional questions relate to how much time it takes for the respondent to wake up in the morning. Total scores range from 21 to 105 and higher scores indicate increased difficulty from tiredness. The change in SIQ score is obtained by subtracting the total score at Day 14 from the baseline score. Scores above 0 signify that the mean score at Day 14 was lower than the mean score at Baseline, indicating reduced difficulty awakening.
Day -1, Day 14
On-Treatment Sleep Inertia Likert Scale
大体时间:Day 1 through Day 14
Sleep inertia is measured with a single item on a 10-point Likert scale asking participants how difficult it was for them to wake up in the morning, where 1 = "not difficult at all" and 10 = "very difficult". The average scores across 14 days are compared between study arms.
Day 1 through Day 14
Change in Interleukin 1 Alpha (IL-1α)
大体时间:Day -1, Day 14
Blood samples are used to determine the change in levels of IL-1α between the study arms. IL-1α is a soporific cytokine and a reduction in soporific cytokines is hypothesized to reduce daytime sleepiness. The change in IL-1α is obtained by subtracting the IL-1α level at Day 14 from the Baseline level.
Day -1, Day 14
Change in Interleukin 1 Beta (IL-1β)
大体时间:Day -1, Day 14
Blood samples are used to determine the change in levels of IL-1β between the study arms. IL-1β is a soporific cytokine and a reduction in soporific cytokines is hypothesized to reduce daytime sleepiness. The change in IL-1β is obtained by subtracting the IL-1β level at Day 14 from the Baseline level.
Day -1, Day 14
Change in Interleukin 2 (IL-2)
大体时间:Day -1, Day 14
Blood samples are used to determine the change in levels of IL-2 between the study arms. IL-2 is a soporific cytokine and a reduction in soporific cytokines is hypothesized to reduce daytime sleepiness. The change in IL-2 is obtained by subtracting the IL-2 level at Day 14 from the Baseline level.
Day -1, Day 14
Change in Interleukin 6 (IL-6)
大体时间:Day -1, Day 14
Blood samples are used to determine the change in levels of IL-6 between the study arms. IL-6 is a soporific cytokine and a reduction in soporific cytokines is hypothesized to reduce daytime sleepiness. The change in IL-6 is obtained by subtracting the IL-6 level at Day 14 from the Baseline level.
Day -1, Day 14
Change in Interleukin (IL-8)
大体时间:Day -1, Day 14
Blood samples are used to determine the change in levels of IL-8 between the study arms. IL-8 is a soporific cytokine and a reduction in soporific cytokines is hypothesized to reduce daytime sleepiness. The change in IL-8 is obtained by subtracting the IL-8 level at Day 14 from the Baseline level.
Day -1, Day 14
Change in Interleukin (IL-15)
大体时间:Day -1, Day 14
Blood samples are used to determine the change in levels of IL-15 between the study arms. IL-15 is a soporific cytokine and a reduction in soporific cytokines is hypothesized to reduce daytime sleepiness. The change in IL-15 is obtained by subtracting the IL-15 level at Day 14 from the Baseline level.
Day -1, Day 14
Change in Interleukin (IL-18)
大体时间:Day -1, Day 14
Blood samples are used to determine the change in levels of IL-18 between the study arms. IL-18 is a soporific cytokine and a reduction in soporific cytokines is hypothesized to reduce daytime sleepiness. The change in IL-18 is obtained by subtracting the IL-18 level at Day 14 from the Baseline level.
Day -1, Day 14
Change in Tumor Necrosis Factor Beta (TNF-β)
大体时间:Day -1, Day 14
Blood samples are used to determine the change in levels of TNF-β between the study arms. TNF-β is a soporific cytokine and a reduction in soporific cytokines is hypothesized to reduce daytime sleepiness. The change in TNF-β is obtained by subtracting the TNF-β level at Day 14 from the Baseline level.
Day -1, Day 14
Change in Interferon Alpha (INF-α2a)
大体时间:Day -1, Day 14
Blood samples are used to determine the change in levels of INF-α2a between the study arms. INF-α2a is a soporific cytokine and a reduction in soporific cytokines is hypothesized to reduce daytime sleepiness. The change in INF-α2a is obtained by subtracting the INF-α2a level at Day 14 from the Baseline level.
Day -1, Day 14
Change in Functional Outcomes of Sleep Questionnaire (FOSQ) Score
大体时间:Day -1, Day 14
The FOSQ is a 30-item instrument assessing how sleepiness impacts daily activities. There are five subscales assessing General Productivity, Activity Level, Vigilance, Social Outcomes, and Intimate and Sexual Relationships. Items are scored on a 4-point scale where 1 = extreme difficulty and 4 = no difficulty. Subscale scores are obtained by calculating the mean score for the items in that subscale and each can range from 1 to 4, where higher scores indicate less difficulty due to sleepiness. A total score is obtained by calculating the means of the subscale scores and multiplying that by the number of subscales with a score. The total score ranges from 5 to 20 and higher scores indicate less difficulty from sleepiness. The change in FOSQ score is obtained by subtracting the total score at Day 14 from the Baseline score. Scores below 0 signify that the mean score at Day 14 was higher than the mean score at Baseline, indicating reduced difficulty from sleepiness.
Day -1, Day 14
Change in Hypersomnia Severity Index (HSI)
大体时间:Day -1, Day 14
The HSI is a 9-item instrument assessing the severity of excessive sleepiness (hypersomnolence). Items are scored on a Likert scale where 0 = not at all and 4 = very much. Total scores range from 0 to 36 and higher scores indicate greater severity of symptoms of hypersomnia. The change from baseline is calculated as the baseline score minus the score at Day 14. The change in HSI score is obtained by subtracting the total score at Day 14 from the baseline score. Scores above 0 signify that the mean score at Day 14 was lower than the mean score at Baseline, indicating reduced severity of hypersomnia symptoms.
Day -1, Day 14
Change in MRI Functional Connectivity
大体时间:Day -2, Day 13
For functional connectivity analyses, each functional scan is parceled into the 246 regions of interest (ROIs), spanning Yeo's 7 networks contained in the Brainnetome Atlas and mean timecourse is calculated for each group. Pearson correlations between each pair of ROIs are calculated, to determine the strength of functional connectivity between each pair of regions and inter/intra-network. This yields a functional connectivity matrix for each functional scan (at both a subject- and group-level). These correlation matrices are Fischer z-transformed and averaged across each condition to create a mean functional connectivity matrix for each condition. Here, the average default mode network (DMN) connectivity is reported. Z-scores have a mean of 0 and scores higher than 0 indicate increased functional connectivity. The change from Baseline is calculated by subtracting the Day 13 score from the score at Day -2. Values lower than 0 mean that the Day 13 score was higher than at baseline.
Day -2, Day 13
Change in MRI Task Performance - N-Back Accuracy
大体时间:Day -2, Day 13
Participants complete a working memory task during functional magnetic resonance imaging (fMRI). The change in task performance is measured as accuracy during 3 different levels of back tasks (0-back, 1-back, and 2-back), from baseline to on-treatment (Day 13). The 0-back test has participants respond to a prespecified stimulus and is a control condition. The 1-back involves remembering and responding to a prior stimulus, while a stimulus two trials earlier is responded to with the 2-back. The change in the percentage of correct responses is obtained by subtracting the percentage at Day 14 from the Baseline percentage. Values below 0 signify that the mean percent accuracy at Day 14 was higher than the mean percent accuracy at Baseline, indicating increased accuracy.
Day -2, Day 13
Change in MRI Task Performance - N-Back Reaction Time
大体时间:Day -2, Day 13
Participants complete a working memory task during functional magnetic resonance imaging (fMRI). he change in task performance is measured as reaction time during 3 different levels of back tasks (0-back, 1-back, and 2-back), from baseline to on-treatment (Day 13). The 0-back test has participants respond to a prespecified stimulus and is a control condition. The 1-back involves remembering and responding to a prior stimulus, while a stimulus two trials earlier is responded to with the 2-back. The change in the reaction time of responses is obtained by subtracting the time at Day 14 from the Baseline time. Scores above 0 signify that the mean time at Day 14 was lower than the mean time at Baseline, indicating faster reaction time.
Day -2, Day 13

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Lynn Marie Trotti, MD, MSc、Emory University

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2019年9月4日

初级完成 (实际的)

2025年6月18日

研究完成 (实际的)

2025年6月18日

研究注册日期

首次提交

2019年7月17日

首先提交符合 QC 标准的

2019年7月18日

首次发布 (实际的)

2019年7月19日

研究记录更新

最后更新发布 (实际的)

2026年8月7日

上次提交的符合 QC 标准的更新

2026年7月16日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

关键字

其他研究编号

  • IRB00108681
  • 1R01NS111280 (美国 NIH 拨款/合同)
  • 2025P011204 (其他标识符:Emory IRB)

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

去识别化后,试验期间收集的个人患者数据将可与其他研究人员共享,这些数据是文章中报告结果的基础。

IPD 共享时间框架

从文章发表后 3 个月开始,到文章发表后 3 年结束,数据将可供共享。 3 年后将做出合理尝试来满足请求。

IPD 共享访问标准

个人参与者数据将可用于与提供方法论合理建议的研究人员以及提供数据使用明确理由的其他实体共享。 将共享数据进行分析,以实现已批准提案的目标。 使用这些数据的建议应发送至 lbecke2@emory.edu。

IPD 共享支持信息类型

  • 研究方案

药物和器械信息、研究文件

研究美国 FDA 监管的药品

是的

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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