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临床试验/NCT06818513
NCT06818513尚未招募不适用

Effects of Gastrostomy and Intermittent Oral Tube Feeding on Patients With Dysphagia After Stroke

Muhammad0 个研究点目标入组 150 人开始时间: 2025年3月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
150
主要终点
Body mass index

研究概览

简要总结

The goal of this clinical trial is to compare the differences in swallowing function, quality of life and nutritional status between ischemic stroke patients with dysphagia using Intermittent Oro-esophageal Tube and Gastrostomy. Patients will be randomly divided into an oral tube group and a Gastrostomy group, all receiving routine rehabilitation treatment. On this basis, the oral tube group will use Intermittent Oro esophageal Tube for enteral nutrition support, while the Gastrostomy group will use Gastrostomy. Researchers will compare changes in swallowing function, quality of life and nutritional status of two groups of patients before and after the study to see if Intermittent Oro-esophageal Tube can improve the quality of life and nutritional status between ischemic stroke patients compared Gastrostomy.

详细描述

This study will last 15 days for each patient. The goal of this clinical trial is to compare the differences in swallowing function, quality of life and nutritional status between ischemic stroke patients with dysphagia using Intermittent Oro-esophageal Tube and Gastrostomy. Patients will be randomly divided into an oral tube group and a Gastrostomy group, all receiving routine rehabilitation treatment. On this basis, the oral tube group will use Intermittent Oro esophageal Tube for enteral nutrition support, while the Gastrostomy group will use Gastrostomy. Researchers will compare changes in swallowing function, quality of life and nutritional status of two groups of patients before and after the study to see if Intermittent Oro-esophageal Tube can improve the quality of life and nutritional status between ischemic stroke patients compared Gastrostomy.

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
否

入选标准

  • •Age>18 years.
  • •Meeting the diagnostic criteria for ischemic stroke .
  • •Dysphagia confirmed by Videofluoroscopic Swallowing Study.
  • •Clear consciousness.
  • •No history of prior stroke.
  • •Stable vital signs.

排除标准

  • •Use of tracheostomy tubes.
  • •Dysphagia that might be caused by other diseases that might cause dysphagia, such as head and neck tumors, traumatic brain injury, myasthenia gravis, etc.
  • •Complicated with severe liver and kidney failure, tumors, or hematological disorders.
  • •Simultaneously in need to undergo other therapy that might affect the outcomes of this study.
  • •Pregnant or nursing females.

研究组 & 干预措施

Oral tube group+routine rehabilitation therapy

Experimental

All patients are provided with routine rehabilitation therapy as follows:

Basic treatment, including corresponding control of risk factors and education on healthy lifestyles.

Swallowing training, including lemon ice stimulation, mendelson maneuver, empty swallowing training, and pronunciation training.

The oral tube group will be given enteral nutritional support with Intermittent Oro-esophageal Tube according to the following procedure. The feeding content was formulated by the nutritionists based on the condition and relevant guidelines to reach the energy demand as 20-25 kcal/kg/day and protein supplementation of 1.2-2.0 g/kg/day for both two groups.

干预措施: routine rehabilitation therapy (Behavioral)

Oral tube group+routine rehabilitation therapy

Experimental

All patients are provided with routine rehabilitation therapy as follows:

Basic treatment, including corresponding control of risk factors and education on healthy lifestyles.

Swallowing training, including lemon ice stimulation, mendelson maneuver, empty swallowing training, and pronunciation training.

The oral tube group will be given enteral nutritional support with Intermittent Oro-esophageal Tube according to the following procedure. The feeding content was formulated by the nutritionists based on the condition and relevant guidelines to reach the energy demand as 20-25 kcal/kg/day and protein supplementation of 1.2-2.0 g/kg/day for both two groups.

干预措施: Oral tube feeding (Dietary Supplement)

Gastrostomy group+routine rehabilitation therapy

Active Comparator

All patients were provided with routine rehabilitation therapy as follows:

Basic treatment, including corresponding control of risk factors and education on healthy lifestyles.

Swallowing training, including lemon ice stimulation, mendelson maneuver, empty swallowing training, and pronunciation training.

The Gastrostomy group will be given enteral nutritional support with Gastrostomy. The feeding content was formulated by the nutritionists based on the condition and relevant guidelines to reach the energy demand as 20-25 kcal/kg/day and protein supplementation of 1.2-2.0 g/kg/day for both two groups

干预措施: routine rehabilitation therapy (Behavioral)

Gastrostomy group+routine rehabilitation therapy

Active Comparator

All patients were provided with routine rehabilitation therapy as follows:

Basic treatment, including corresponding control of risk factors and education on healthy lifestyles.

Swallowing training, including lemon ice stimulation, mendelson maneuver, empty swallowing training, and pronunciation training.

The Gastrostomy group will be given enteral nutritional support with Gastrostomy. The feeding content was formulated by the nutritionists based on the condition and relevant guidelines to reach the energy demand as 20-25 kcal/kg/day and protein supplementation of 1.2-2.0 g/kg/day for both two groups

干预措施: Gastrostomy (Dietary Supplement)

结局指标

主要结局

Body mass index

时间窗: day 1 and day 15

body mass index will be calculated as body weight/height\^2.

次要结局

  • Dysphagia Handicap Index(day 1 and day 15)
  • Modified Barium Swallow Impairment Profile(day 1 and day 15)
  • Penetration-Aspiration Scale(day 1 and day 15)

研究者

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

Muhammad

The Research Director

Ahmadu Bello University Teaching Hospital

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