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
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