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临床试验/NCT04061577
NCT04061577终止不适用

Transcranial Electrical Stimulation in Stroke EaRly After Onset Clinical Trial_ Bridging and Adjunctive Neuroprotection

University of California, Los Angeles2 个研究点 分布在 1 个国家目标入组 1 人开始时间: 2019年7月28日最近更新:
适应症

试验速览

阶段
不适用
状态
终止
入组人数
1
试验地点
2
主要终点
Primary Safety Outcome- Number of Participants With Symptomatic Intracranial Hemorrhage (SICH)

研究概览

简要总结

This proposal is a prospective, single-center, dose-escalation safety, tolerability, feasibility and potential efficacy study of transcranial direct current stimulation (tDCS) in acute stroke patients with substantial salvageable penumbra due to a large vessel occlusion before and after endovascular therapy.

详细描述

This is a single-center, sham-controlled, dose-escalation study where cathodal tDCS is delivered to threatened but not yet irreversibly damaged (penumbral) tissue in patients with large vessel occlusion who are undergoing recanalization procedure. Patients will be randomized in a 3:1 design, to cathodal versus sham (control) stimulation, at each six designed dose tiers. The dose tiers will be increasing in both intensity and duration of the stimulation. All patients will be receiving the first dose (stimulation cycle) after the recanalization procedure and patients at dose tiers 5-6 will also be receiving stimulation cycles before the recanalization procedure begins.

The occurrence of symptomatic intracranial hemorrhage will determine the pace of the escalation through the dose tiers.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Treatment
盲法
Single (Participant)

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

结局指标

主要结局

Primary Safety Outcome- Number of Participants With Symptomatic Intracranial Hemorrhage (SICH)

时间窗: At 24-hour post-stimulation

Symptomatic intracranial hemorrhage (SICH) is defined as an increase of 4 or more points on the National Institute of Health Stroke Scale (NIHSS) total score within 24 hours of stimulation associated with parenchymal hematoma type 1 (PH1), parenchymal hematoma type 2 (PH2), remote intraparenchymal hemorrhage (RIH), subarachnoid hemorrhage (SAH), or intraventricular hemorrhage (IVH). The NIHSS is a 15-item neurologic examination stroke scale used to evaluate the effect of acute stroke on the levels of consciousness, language, neglect, visual-field loss, extraocular movement, motor strength, ataxia, dysarthria, and sensory loss. A trained observer rates the patent's ability to answer questions and perform activities. Ratings for each item are scored with 3 to 5 grades with 0 as normal, and there is an allowance for untestable items. Accordingly, 0 is the lowest and 42 is the highest total score possible. In the NIHSS, the higher the score, the more impaired a stroke patient is.

Primary Tolerability Outcome-Number of Participants Completing the Protocol-assigned Stimulation

时间窗: After 5 minutes of stimulation period

The percentage of the patients completing the protocol-assigned stimulation treatment with no intolerability.

Primary Feasibility Outcome- Assessing the Speed of Stimulation Implementation From Randomization.

时间窗: Median time from randomization to tDCS initiation

The median times from randomization to bridging C-tDCS initiation and the time form end of endovascular thrombectomy procedure to adjunctive C-tDCS initiation in the last 10 enrolled patients.

次要结局

  • Secondary Safety Outcome-Number of Participants With All Serious Adverse Events (Anticipated and Unanticipated)(At 90 days post-stimulation)
  • Secondary Safety Outcome-Number of Participants With Asymptomatic Intracranial Hemorrhage (AICH)(At 24-hour post-stimulation)
  • Secondary Safety Outcome-Number of Participants With Early Neurologic Deterioration(At 24-hour post-stimulation)
  • Secondary Safety Outcome-Number of Participants With Mortality(At 90 days post-stimulation)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mersedeh Bahr Hosseini, MD

Principal Investigator

University of California, Los Angeles

研究点 (2)

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