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临床试验/PER-016-04
PER-016-04已完成未知

PHOTOTHERA LASER SYSTEM FEASIBILITY ASSESSMENT

PHOTOTHERA INC.,0 个研究点目标入组 0 人开始时间: 2004年4月21日最近更新:

试验速览

阶段
未知
状态
已完成

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
0 至 0(—)

入选标准

  • The Subject is at least 40 years old at the time of detection, but has not reached his 85th birthday.
  • The Subject suffers from acute ischemic stroke.
  • Possibility of starting treatment with photothera laser system within 24 hours of the start of the ACV
  • The subject and / or his / her legal representative give their informed consent before taking the study.
  • The Subject wishes to participate in this study for at least 3 months after the start of the ACV.

排除标准

  • The Subject has been presented to the Community hospital more than 24 hours after the start of the ACV.
  • Evidence of intracranial, subdural or subarachnoid hemorrhage in the CT scan
  • The subject is a candidate for intravenous administration of tissue plasminogen activator (tPA) for the treatment of acute ischemic stroke and is administered tPA.
  • The Subject had convulsions at the beginning of the ACV.
  • Serum glucose greater than 400 mg / dL or less than 40 mg / dL.

研究者

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