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Clinical Trial Summary

The main question it aims to answer are: 1. whether the new target delineation scheme can improve Progression-free Survival 2. whether it can reduce the incidence of radiation complications in high-grade glioma patients. Participants in trial group will be performed radiotherapy of new target delineation method after the completion of the operation within 4-6 weeks., while participants in the control group be performed radiotherapy of EORTC(European organisation for research and treatment of cancer) target delineation method.Temozolomide 75 mg / ( m² · d ) will be given to both groups of patients during radiotherapy. After radiotherapy, its dose changes to 150 ~ 200 mg / ( m² · d ) for 5 days and stopped for 23 days as a cycle. There are 6 cycles in total.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06215495
Study type Interventional
Source Zhujiang Hospital
Contact Yujing Tan, Doctor
Phone +8613560347303
Email tanyujing-1981@163.com
Status Recruiting
Phase N/A
Start date February 18, 2024
Completion date June 1, 2027

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