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Study identifier: NCT07657403 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

CONNEctome-guided Navigation for Eloquent-area Tumor Surgery Trial

Condition: Brain Neoplasms · Eloquent Area Brain Tumors  ·  Sponsor: Cancer Institute and Hospital, Chinese Academy of Medical Sciences

PhaseNA
Planned participants200
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

This study is designed for patients with brain tumors located in eloquent brain areas involved in language, motor, or major functional brain networks. The purpose of the study is to determine whether connectome-guided navigation-assisted microsurgical resection can better preserve neurological function after surgery than conventional tractography-guided surgery. Participants who meet the study criteria will be assigned to one of two surgical planning strategies. In the experimental group, patients will undergo preoperative diffusion tensor imaging and resting-state functional MRI for individualized brain network reconstruction, and these data will be integrated with intraoperative navigation and neurophysiological monitoring to guide the resection boundary. In the control group, surgery will be guided by conventional DTI tractography-assisted navigation. The main outcome is the rate of postoperative functional preservation. Other outcomes include extent of tumor resection, postoperative complications, time to neurological recovery, overall survival, and quality of life. Patients will be evaluated before surgery and followed after surgery with clinical examinations, neurological assessments, and MRI at prespecified time points.

This description comes directly from the study's public registry record.

Talk to the study team

Fengchun Mu  ·  +8618888294650  ·  alicemfc@163.com

Always discuss trial participation with your own doctor first.

Locations (1)

National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical CollegeBeijing, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07657403