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临床试验/CTRI/2024/02/062273
CTRI/2024/02/062273招募中2/3 期

Memantine to preserve memory and neurocognition following craniospinal irradiation (MEMENTO)- A randomised control trial

Tata Memorial Hospital1 个研究点 分布在 1 个国家目标入组 101 人开始时间: 2024年2月22日最近更新:

试验速览

阶段
2/3 期
状态
招募中
入组人数
101
试验地点
1
主要终点
Cognitive-deterioration-free survival

研究概览

简要总结

Craniospinal irradiation  involving radiation of brain and spine, along with tumor-bed boost with or without chemotherapy, is the current standard treatment for medulloblastoma and other primitive embryonal tumors of the central nervous system. The delayed side effects following CSI include memory loss, hearing and balance difficulties, hormonal imbalance, and secondary cancers. Decline in memory severely affects the quality of life in long term survivors of these diseases. Hence, various strategies are being tried to prevent it. Memantine has been proven to effectively prevent the memory decline induced by RT. It is FDA-approved for Alzheimer’s disease and is widely used in the children for several developmental disorders. With this study, we are trying to investigate the role of memantine in patients receiving CSI to prevent memory decline.

After screening for the study, eligible patients will be randomly allocated by computerised system to one of the two arms that are described as follows. Patients in the experimental arm memantine will be started on memantine, starting dose of the same will be 5mg once daily at bedtime for 1 week, followed by 5mg twice daily for 1 week, and finally increased to the full dose of 10 mg twice daily for 6 months. Patients will continue radiation and chemotherapy when indicated as per schedule. All patients in the study will undergo neurocognitive evaluation, the time points for which will be pre-radiation baseline, 6 months post-RT, 1-year post-RT, and annually after that for 5 years from radiation. Following completion of RT or treatment, standard follow-up protocols will include a clinical examination 3 monthly for the first 2 years, followed by 6 monthly visits till 5 years post-RT. No additional risk is expected from the current study other than the common side effects of the standard treatment. Based on the results from the study, if primary endpoints are achieved, it will establish the role of memantine in preventing memory decline from CSI, which can be used as a standard treatment measure to help patients in the future.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
5.00 Year(s) 至 39.00 Year(s)(—)
性别
All

入选标准

  • Planned for CSI, with or without boost dose with or without systemic chemotherapy Informed consent or assent taken Karnofsky Performance Status, Lanksy Performance Status≥60.

排除标准

  • Re-irradiation Prior exposure to memantine Inability to undergo Wechsler test.

结局指标

主要结局

Cognitive-deterioration-free survival

时间窗: 2yrs after accrual

次要结局

  • Overall survival (OS)(at the completion of the study)
  • Progression free survival (PFS)(until progression at any time point during the study)

研究者

申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Dr Tejpal Gupta

Tata Memorial Hospital

研究点 (1)

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