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临床试验/IRCT20200609047706N1
IRCT20200609047706N1招募中3 期

Effect of Citicoline on Barthel Index in Patients with Moderate and Severe Traumatic Brain Injury

Esfahan University of Medical Sciences0 个研究点目标入组 80 人开始时间: 待定最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
80

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
no limit 至 no limit(—)
性别
All

入选标准

  • Patients with severe and moderate traumatic brain injury based on GCS less than 12
  • Patients should be without traumatic major lesions in the thorax, abdomen, and limbs
  • Patients without heart problems
  • Have the satisfaction to enter the study

排除标准

  • Previous history of brain Injury, stroke, or neurological disease
  • Contraindications or sensitivity to Citicoline
  • The presence of comorbidities such as cardiovascular, renal, hepatic, and malignant history
  • Traumatic brain injury, major trauma to the thorax, abdomen and other organs
  • Unstable hemodynamics
  • Surgical interventions were performed within the first 24 hours after trauma
  • cardiopulmonary resuscitation was performed within the first 24 hours after trauma
  • Dissatisfaction of the patient to enter the study and her/his death during the study

研究者

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