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临床试验/NCT04221256
NCT04221256撤回1 期

Dose-finding Study of Selective Serotonin Reuptake Inhibitors to Enhance Neuroplasticity

Burke Medical Research Institute1 个研究点 分布在 1 个国家开始时间: 2020年3月11日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
撤回
发起方
试验地点
1
主要终点
Change in motor evoked potential amplitude

研究概览

简要总结

The brain is able to change throughout life in response to learning, or injury, or to adapt to changes in the environment, which is known as neuroplasticity. Stroke survivors suffer disabling chronic motor impairments that have proven challenging to improve. Increasing neuroplasticity using selective serotonin reuptake inhibitors (SSRIs) is a promising approach to promote motor recovery in patients with stroke.

详细描述

The brain is able to change throughout life in response to learning, or injury, or to adapt to changes in the environment, which is known as neuroplasticity. Stroke survivors suffer disabling chronic motor impairments that have proven challenging to improve. Increasing neuroplasticity using selective serotonin reuptake inhibitors (SSRIs) is a promising approach to promote motor recovery in patients with stroke. Selective serotonin reuptake inhibitors (SSRIs) are currently widely used for treatment of depression, but they also have been shown to be able to enhance neuroplasticity. A single dose of SSRI has been shown to improve hand function in patients with chronic stroke. SSRIs also enhance neuroplasticity in healthy individuals, as shown using paired associative stimulation (PAS), a non-invasive method which causes the brain's excitability to change. However, the best dose of SSRI to increase neuroplasticity is not yet established.

The purpose of this study is to (1) find the effective dose of the SSRI escitalopram to modulate PAS-induced plasticity in patients with stroke and healthy individuals and (2) determine the variability of escitalopram's effect on PAS-induced plasticity between individuals. We measure neuroplasticity with PAS, which causes the brain's excitability to change. During PAS, you would receive electrical stimulation over your wrist and magnetic stimulation to their scalp (called transcranial magnetic stimulation, or TMS) to increase the excitability of the motor area of the brain. You will be asked to participate in a screening visit and 8 study visits separated by at least 1 week. At each study visit, you will be given a single dose of escitalopram (5, 10 or 20) or placebo, and we will measure your brain's change in excitability after PAS.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Administration of SSRI

Experimental

Participants will be administered either 5, 10 or 20mg of SSRI escitalopram prior to paired associative stimulation.

干预措施: Administration of SSRI escitalopram (Drug)

Administration of SSRI

Experimental

Participants will be administered either 5, 10 or 20mg of SSRI escitalopram prior to paired associative stimulation.

干预措施: Paired Associative stimulation (Behavioral)

Administration of Placebo

Placebo Comparator

Participants will be administered a placebo prior to paired associative stimulation

干预措施: Paired Associative stimulation (Behavioral)

Administration of Placebo

Placebo Comparator

Participants will be administered a placebo prior to paired associative stimulation

干预措施: Administration of Placebo (Drug)

结局指标

主要结局

Change in motor evoked potential amplitude

时间窗: Baseline, Up to 30 minutes Post PAS

Assessment of corticospinal excitability

次要结局

未报告次要终点

研究者

发起方
Burke Medical Research Institute
申办方类型
Other
责任方
Principal Investigator
主要研究者

Tomoko Kitago

Lab Director Human Motor Recovery Laboratory Assistant Professor

Burke Medical Research Institute

研究点 (1)

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