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临床试验/TCTR20210902001
TCTR20210902001已完成2 期

Immunonutrition Supplement for Reducing Acute Oral Mucositis in Head and Neck Cancer Radiotherapy

Division of Radiotherapy and Oncology0 个研究点目标入组 100 人开始时间: 2021年9月2日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 70 Years(—)
性别
All

入选标准

  • 1.Age range between 18 - 70-year-old
  • 2.Histologically confirmed squamous cell carcinoma of head and neck.
  • 3.Locally advanced head and neck cancer planning to treat with concurrent chemoradiotherapy for definitive or postoperative setting.
  • 4.No previous radiotherapy in head and neck area.
  • 5.Good performance status with ECOG 0-1.
  • 6.Laboratory tests are in the normal ranges.
  • 7.The participant or legal representative provides the written informed consent for the study.

排除标准

  • 1.Histological subtypes other than squamous cell carcinoma (e.g., Adenocarcinoma, small cell carcinoma).
  • 2.Has metastatic disease or locoregional recurrence.
  • 3.Receive immune-enhancing nutrition product prior to the randomization within 30 days.
  • 4.Allergy to immune-enhancing nutrition ingredients used in the study.
  • 5.Active autoimmune disease(s) that require medication within 2 years.
  • 6.Diabetes Mellitus, renal disease, liver disease and/or other disease that limits some nutrition or calorie intake.
  • 7.Known disease or condition that would interfere with the cooperation of the study.
  • 8.Pregnancy or breastfeeding.

研究者

发起方
Division of Radiotherapy and Oncology

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