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临床试验/NCT02983942
NCT02983942Unknown1 期

Ketogenic Diet Adjunctive to High Dose Methotrexate Chemotherapy for Primary Central Nervous System Lymphoma

Beijing Tiantan Hospital1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2017年1月1日最近更新:
适应症

试验速览

阶段
1 期
发起方
入组人数
50
试验地点
1
主要终点
Number of participants with treatment related adverse events as assessed by CTCAE v4.0

研究概览

简要总结

Ketogenic diet has shown auxiliary effect on treatment of malignant tumors require high glucose consumption. This study is designed to evaluate the safety and efficacy of ketogenic diet adjunctive to high dose methotrexate(HD-MTX) chemotherapy for primary central nervous system lymphoma (PCNSL).

详细描述

In a pilot study of primary central nervous system(CNS) lymphoma patients, ketogenic diet was given in adjunction with standard HD-MTX chemotherapy as interventional group; standard HD-MTX is given with routine diet as control group. The primary endpoint is the safety of ketogenic diet in PCNSL patients receiving chemotherapy, secondary endpoints include rate of complete remission, remission time, rate of tumor relapse and overall survival.

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histopathologically confirmed PCNSL
  • No systemic involvement
  • Ability and willingness to sign informed consent
  • Normal liver and kidney function
  • Karnofsky Performance Score of 60 or more

排除标准

  • Any systemic involvement of the tumor
  • Systemic illness or medical condition may pose additional risk, including cardiac, metabolic or endocrine disorders; incompensated renal or liver disfunction; history of renal calculi, hyperuricemia, hyper calcemia, mitochondrial disease, known disorder of fatty acid metabolism, porphyria, carnitine deficiency and pancreatitis
  • Uncontrolled hyperlipidemia or hyperglycemia
  • Human immunodeficiency virus positive, or hepatitis C positive
  • Pregnancy of breastfeeding
  • Inability or unwillingness to give written informed consent.

结局指标

主要结局

Number of participants with treatment related adverse events as assessed by CTCAE v4.0

时间窗: Two years

The number and incidence (%) of treatment related adverse events among participants

次要结局

  • The chemosensitivity of tumor(Two years)
  • Long term effect of chemotherapy(Two years)
  • overall survival(Three years)
  • Quality of life(Two years)

研究者

发起方
Beijing Tiantan Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Song Lin

Professor

Beijing Tiantan Hospital

研究点 (1)

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