ITMCTR2100004944招募中1 期
Clinical study on prevention and treatment of radiation acute oral mucositis in patients with nasopharyngeal carcinoma by self-prepared Chinese herbal compound preparation
Affiliated Hospital of Chengdu University of Traditional Chinese Medicine0 个研究点开始时间: 待定最近更新:
试验速览
- 阶段
- 1 期
- 状态
- 招募中
- 发起方
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional study
入排标准
- 年龄范围
- 18 至 70(—)
- 性别
- All
入选标准
- •1. Patients with locally advanced nasopharyngeal carcinoma diagnosed by pathology and UICC/AJCC TNM staging of stage III and stage A in the 8th edition;
- •2. Has indications for radical concurrent radiotherapy and chemotherapy, and is scheduled to receive (IMRT technique for radiotherapy, platinum-containing regimen for chemotherapy), and has received radiotherapy for the first time, and has not received surgical treatment;
- •3. Kanofsky Performance Status (KPS) score >= 70;
- •4. Blood routine, normal liver and kidney function, and good blood glucose control in diabetic patients (fasting blood glucose 3.9-7.2mmol/L, blood glucose 2 hours after meal <= 10.0mmol/L, HbA1c < 7%);
- •5. Expected survival of at least 6 months;
- •6. Age between 18 and 70 years old, male or female;
- •7. Signing the informed consent.
排除标准
- •1. Pregnant women, lactating women, and women of childbearing age who were unable to obtain effective contraception during the trial;
- •2. Other established oral mucosal diseases and no previous history of salivary gland diseases;
- •3. Patients with recurrent or residual nasopharyngeal carcinoma;
- •4. Complicated with serious heart, liver, kidney, hematopoietic system and nervous system diseases, diabetes mellitus with unsatisfactory blood glucose control and mental disorders;
- •5. Patients with other malignant tumors;
- •6. People who are known or suspected to be allergic to the drugs in this study;
- •7. Other circumstances that the researcher considers not suitable for the study.
研究者
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