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临床试验/NCT06249022
NCT06249022Unknown不适用

A Randomized Controlled Study to Explore the Effect of Different Feeding in Traumatic Brain Injury Patients

Zeng Changhao1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年2月20日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
100
试验地点
1
主要终点
Concentration of hemoglobin

研究概览

简要总结

This was a multicenter randomized controlled study of 98 severe Traumatic Brain Injury patients with tracheostomy. Patients enrolled were divided randomly into the observation group with Intermittent Oro-esophageal Tube Feeding or the control group with Nasogastric tube feeding for enteral nutrition support, respectively. Nutritional status, complications, decannulation of tracheostomy tubes and level of consciousness on day 1 and day 28 were recorded and compared.

详细描述

The safe and effective nutrition support for severe traumatic brain injury patients with tracheostomy continues to be a challenge. Nasogastric tube feeding has been the mainstream choice in China but with the risk of complications. Intermittent Oro-esophageal Tube Feeding is an established modality of enteral nutrition support that can be used with routine treatment. This study reports the clinical outcomes of Intermittent Oro-esophageal Tube Feeding vs. nasogastric tube feeding, in patients receiving routine treatment. This was a multicenter randomized controlled study of 98 severe traumatic brain injury patients with tracheostomy. Patients enrolled were divided randomly into the observation group with Intermittent Oro-esophageal Tube Feeding or the control group with Nasogastric tube feeding for enteral nutrition support, respectively. Nutritional status, complications, decannulation of tracheostomy tubes and level of consciousness on day 1 and day 28 were recorded and compared.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Double (Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • age ≥ 18 years, meeting the diagnosis of severe Traumatic Brain Injury, confirmed through MRI
  • score of Glasgow Coma Scale (GCS) <8;
  • presence of no contraindication for enteral nutrition;
  • with stable vital signs and no severe liver or kidney dysfunction, metabolic disorders, cardiovascular diseases, or multiple complications;
  • informed consent form was obtained from the patients' family members.

排除标准

  • unable to cooperate in completing treatment and assessment due to personal reasons or other disorders;
  • complicated with other intracranial lesions, such as stroke;
  • with severe consciousness disorders caused by other diseases.

结局指标

主要结局

Concentration of hemoglobin

时间窗: day 1 and day 28

hemoglobin was tested with blood routine test

Concentration of albumin

时间窗: day 1 and day 28

albumin was tested with blood routine test

Concentration of prealbumin

时间窗: day 1 and day 28

prealbumin was tested with blood routine test

body mass index

时间窗: day 1 and day 28

body mass index was tested with body weight and height. Combination was calculated as: body weight (kg) / height (m)\^2.

次要结局

  • Decannulation of tracheostomy tube-placement duration(day 1 and day 28)
  • Decannulation of tracheostomy tube-Successful removal(day 1 and day 28)
  • Level of consciousness(day 1 and day 28)
  • Feeding Amount(day 1 and day 28)

研究者

发起方
Zeng Changhao
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Zeng Changhao

Research Director

People's Hospital of Zhengzhou University

研究点 (1)

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