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临床试验/TCTR20240325005
TCTR20240325005已完成2 期

Clinical outcome and safety of neuromodulation for severe traumatic brain injury in terms of neurological recovery

Phramongkutklao hospital foundation0 个研究点目标入组 68 人开始时间: 2024年3月25日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
68

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20 Years 至 N/A (No limit)(—)
性别
All

入选标准

  • 1. all the adult patients with severe disability (GOS of 2 and 3) after trauma or stroke
  • 2. Age more than 20 years
  • 3. Patients have focal neurological deficits presenting with magnetic resonance imaging (MRI) brain or computed tomography (CT) head suggestive of MCA territory AIS presenting within 24 hour of symptom onset, National Institute of Health Stroke Scale (NIHSS) score of >4 and with a modified Rankin Scale (mRS) score of 0 or 1 before the stroke were included in this study.

排除标准

  • Patients with brainstem strokes, transient ischemic attacks, brain tumor, demyelinating diseases, inflammatory diseases, craniotomies, hepatic failure, congestive heart failure, acute myocardial infarction, pregnancy and lactation, systemic malignancy, acute or chronic renal failure, and known allergy to above group of drugs.

研究者

发起方
Phramongkutklao hospital foundation

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