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临床试验/NCT06328985
NCT06328985已完成不适用

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

Zeng Xi2 个研究点 分布在 1 个国家目标入组 98 人开始时间: 2024年3月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
98
试验地点
2
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
Single (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.

研究组 & 干预措施

Rehabilitation therapy+Intermittent Oro-esophageal Tube Feeding

Experimental

Both groups of patients were provided with routine treatments, including pharmacological treatment, rehabilitation therapy.Based on this, the patients in the observation group were given enteral nutrition support with Intermittent Oro-esophageal Tube Feeding (Medical Device No. 20010234, developed by the Swallowing Disorders Research Institute of Zhengzhou University).

干预措施: Rehabilitation therapy (Behavioral)

Rehabilitation therapy+Intermittent Oro-esophageal Tube Feeding

Experimental

Both groups of patients were provided with routine treatments, including pharmacological treatment, rehabilitation therapy.Based on this, the patients in the observation group were given enteral nutrition support with Intermittent Oro-esophageal Tube Feeding (Medical Device No. 20010234, developed by the Swallowing Disorders Research Institute of Zhengzhou University).

干预措施: Intermittent Oro-esophageal Tube Feeding (Device)

Rehabilitation therapy+Nasogastric tube feeding

Active Comparator

Both groups of patients were provided with routine treatments, including pharmacological treatment, rehabilitation therapy. The patients in the control group were provided nutrition support with Nasogastric tube feeding , while the feeding process strictly followed the relevant guideline

干预措施: Rehabilitation therapy (Behavioral)

Rehabilitation therapy+Nasogastric tube feeding

Active Comparator

Both groups of patients were provided with routine treatments, including pharmacological treatment, rehabilitation therapy. The patients in the control group were provided nutrition support with Nasogastric tube feeding , while the feeding process strictly followed the relevant guideline

干预措施: Nasogastric tube feeding (Device)

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-Successful removal(day 1 and day 28)
  • Decannulation of tracheostomy tube-placement duration(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 Xi
申办方类型
Other Gov
责任方
Sponsor Investigator
主要研究者

Zeng Xi

The Research Director

Chao Phya Abhaibhubejhr Hospital

研究点 (2)

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