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临床试验/NCT05823272
NCT05823272Unknown不适用

Effect of Oral Nutritional Supplement on Nutritional Status and Clinical Outcome in Gastric Cancer Patients After Total Gastrectomy

Jinling Hospital, China1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年3月22日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
60
试验地点
1
主要终点
incidence of sarcopenia 6-month after discharge

研究概览

简要总结

Gastric cancer patients after total gastrectomy will be randomized to oral nutritional supplement group or control group at discharge. Patients will receive 6 months of oral nutritional supplement or normal diet after discharge. The primary and secondary outcomes will be collected.

详细描述

Gastric cancer patients after total gastrectomy at discharge, if she/he has nutrition risk (NRS2002≥3), then she/he will be randomized to oral nutritional supplement (ONS) group or control (C) group after discharge. In the ONS group, in addition to diet, and patients will also consume enteral nutritional powder (500ml/d,500kcal/d) lasted for 6 months. In the C group, patients will receive normal diet. Both groups will receive nutrition counseling.

The primary and secondary outcomes will be collected.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Informed consent of patients or their legal representatives to participate in this study
  • consecutive adult (18-80 years) patients underwent radical gastrectomy (total gastrectomy)
  • nutrition Risk Screening (NRS) 2002≥3 at discharge
  • eastern Cooperative Oncology Group (ECOG) score of 0-2 at discharge
  • normal liver and kidney function

排除标准

  • unable to oral or consume ONS
  • allergy to any ingredient in the oral nutrition powder
  • palliative surgery or gastric stump cancer
  • congenital acquired immune deficiency disease
  • severe liver and kidney diseases including active hepatitis, cirrhosis, and uremia diabetes has developed complications or uncontrolled by medications
  • motor system diseases cannot complete grip strength measurement and 5-time chair stand test
  • have cognitive impairment, unable to complete the relevant questionnaires
  • expected to require tube feeding after discharge from the hospital

研究组 & 干预措施

control

No Intervention

In the control group, patients will receive nutrition counseling in addition to diet.

oral nutritional supplement

Experimental

In the oral nutritional supplement group, in addition to diet, and patients will also consume enteral nutrition powder (500 ml/d, 500kcal/d) lasted for 6 months after discharge.

干预措施: ONS (Other)

结局指标

主要结局

incidence of sarcopenia 6-month after discharge

时间窗: up to 6 months.

sarcopenia is defined as low skeletal muscle mass plus low muscle strength or low physical ability.

次要结局

  • incidence of sarcopenia 1 year after discharge(up to 12 months.)
  • unplanned readmission rate(up to 6 months.)
  • Quality of life after discharge(up to 12 months.)
  • Changes in BMI (weight and height will be combined to report BMI in kg/m^2)(up to 12 months.)
  • toxicity of chemotherapy graded according to the CTCAE, version 5.0(up to 6 months.)

研究者

发起方
Jinling Hospital, China
申办方类型
Other
责任方
Principal Investigator
主要研究者

Wang Xinying

Prof.

Jinling Hospital, China

研究点 (1)

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