A Multicenter, Single Arm Trial to Assess Safety and Signal of Efficacy of the Ischemic Stroke System (ISS), as an Adjunct to Standard of Care in Subjects With Mild Acute Ischemic Stroke
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 50
- 试验地点
- 8
- 主要终点
- NIHSS Assessment
研究概览
简要总结
Study Population:
Subjects with Mild Acute Ischemic Stroke in the anterior circulation within 24 hours from onset.
Study objectives:
- Identify the personal stimulation level for each patient based on physiological biomarkers
- Identify improvement in stroke symptoms during ISS treatment at the personal stimulation level
详细描述
A Multicenter, Single Arm Trial to Assess Safety and Signal of Efficacy of the Ischemic Stroke System (ISS), as an Adjunct to Standard of Care in Subjects with Mild Acute Ischemic Stroke
Study Duration:
The expected total duration of the study for each subject is up to 10 days as follows:
Enrollment: up to 24 hours Treatment: Implantation, 5 Days of SPG stimulation and Standard of care Final Visit: 7 days after enrollment
Study Population:
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 80 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Age: ≥ 18 years and ≤ 80 years
- •Clinical diagnosis of anterior circulation stroke
- •Baseline NIHSS ≥ 1 and ≤ 6 or lacunar stroke of any severity
- •Motor and/or sensory deficits
- •Ability to initiate treatment within 24 hours from stroke onset
- •Signed informed consent from patient him/herself or legally authorized representative if applicable.
排除标准
- •Neuro-imaging evidence of any intracranial hemorrhage or hemorrhagic transformation of brain infarct or other significant abnormality (e.g. tumor, abscess, suspect for subarachnoid hemorrhage).
- •Massive stroke, defined as acute parenchymal lesion with effacement of cerebral sulci in over 2/3 of the MCA territory.
- •Clinical signs and symptoms or evidence for a relevant lesion by neuro-imaging of an acute ischemic stroke in the posterior circulation (Vertebral, Basilar and/or Posterior Cerebral Artery territories), including but not limited to brain-stem findings and/or cerebellar findings and/or isolated homonymous hemianopia or cortical blindness.
- •NIHSS level of consciousness score ≥
- •Inability to communicate fluently and express symptoms
- •Previous motor and/or sensory deficits that will eliminate the ability to identify the response to SPG stimulation
- •Patients with bleeding propensity and/or one of the following: INR > 1.8, prolonged activated partial thromboplastin time (aPTT) ≥ 45 sec., platelets count < 75×109/L.
- •Known cerebral arteriovenous malformation, cerebral aneurysm.
- •Seizure at onset.
- •Blood glucose concentration < 60 mg/dL.
- •Clinical suspicion of septic embolus.
- •Uncontrolled hypertension (systolic >185 mmHg and/or diastolic >110 mmHg), demonstrated on each of three repeated measurements taken within one hour regardless of whether or not the patient is taking antihypertensive medications.
- •Serious systemic infection.
- •Women known to be pregnant or having a positive or indeterminate pregnancy test.
- •Patients with other implanted neural stimulator/ electronic devices (pacemakers).
- •History of SPG ablation ipsilateral to the stroke side.
- •Any condition in the oral cavity that prevents implantation of the INS, such as patient is intubated, orthodontics or non-hygienic condition.
- •Life expectancy < 1 year from causes other than stroke.
- •Participating in any other therapeutic investigational trial within the last 30 days.
- •Known sensitivity to any medications to be used during study.
- •Subjects who have a clinically significant or unstable medical or surgical condition that may preclude safe and complete study participation. Conditions may include: cardiovascular, vascular, pulmonary, hepatic, renal or neurological (other than acute ischemic stroke), or neoplastic diseases, as determined by medical history, physical examination, laboratory tests, or ECG.
- •Subjects who, in the judgment of the investigator, are likely to be non- compliant or uncooperative during the study.
结局指标
主要结局
NIHSS Assessment
时间窗: Day 7
The difference in NIHSS between baseline and Day 7 vs. Historical Controls (the historical controls are patients in the control arm in the NINDS trial)
% of patients with improvement in stroke symptoms during stimulation
时间窗: Day 2-5
Assessment of improvement in stroke symptoms (motor and/or sensory deficits) before and during stimulation at the Personal Stimulation Level, using a hand dynamometer (Baseline Hydraulic Hand Dynamometers, Fabrication Enterprises Inc, White Plains NY, USA).
次要结局
未报告次要终点