跳至主要内容
临床试验/NCT02988102
NCT02988102Unknown不适用

Role of Concentration of Biomarkers S100B and NSE in Serum in Mild and Moderate Head Trauma Injury in Acute Phase in Relation to Head CT and Post Concusion Syndrome.

University Clinical Centre of Kosova1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2016年12月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
70
试验地点
1
主要终点
Role of concentration of biomarkers S100B and NSE in serum in mild and moderate head trauma injury in acute phase in relation to head CT and post concusion syndrome.

研究概览

简要总结

In pediatric age groups communication difficulties very sometimes may present further obstacles in obtaining a detailed injury history and early identification of TBI symptoms.

Most emergency management protocols are focused exclusively on the identification of the relatively small number of patients who may require operative intervention, as early surgery is believed to improve outcome.

详细描述

However early rehabilitation can also be effective for the much larger number of patients who do not require surgery[1] In addition, Hall and others recently reported that low doses of ionizing radiation to the brain in infancy may influence cognitive abilities in adulthood. [2] Accordingly, increased serum concentrations of, for example S100B ( a calcium-binding protein present in high concentrations in glial cells) and neurone-specific enolase ( NSE: a cytoplasmatic enzyme occuring predominantly in neurones ) have been demonstrated to reflect the presence and severity of brain tissue damage in acute head injuries. [3] In both pediatric age and adults.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
1 Year 至 65 Years(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Only head trauma without any other body injury

排除标准

  • Blood thinner, hydrocephalus , previous brain infarcts, encephalopathy, birth trauma.

结局指标

主要结局

Role of concentration of biomarkers S100B and NSE in serum in mild and moderate head trauma injury in acute phase in relation to head CT and post concusion syndrome.

时间窗: 2 years

次要结局

未报告次要终点

研究者

发起方
University Clinical Centre of Kosova
申办方类型
Other
责任方
Principal Investigator
主要研究者

Dr. Fatos Kelmendi

Dr. Fatos Kelmendi Neurosurgeon

University Clinical Centre of Kosova

研究点 (1)

Loading locations...

相似试验