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NCT06885333

Whole-Brain Tumor Burden Metrics with Inflammatory and Molecular Markers to Predict Postoperative Neurocognitive Decline in Glioma

Completed Last updated 20 March 2025
What this trial tests

trial in Glioma in 192 participants. Completed in 1 December 2024.

Timeline
1 May 2016
Primary endpoint
1 September 2024
1 December 2024

Quick facts

Lead sponsorWest China Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment192
Start date1 May 2016
Primary completion1 September 2024
Estimated completion1 December 2024

Conditions studied

Sponsor

West China Hospital

Who can join

Adults 18 to 65, any sex, with Glioma or Glioma : Oligodendroglioma or Astrocytoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Although surgical resection improves overall survival in patients with diffuse Low-grade gliomas (DLGG), it can also result in deterioration of neurocognitive function, which are poorly understood and lack effective predictive models. This study aims to develop a model using whole-brain tumor burden metrics, inflammatory and molecular markers for predicting high risk of neurocognitive decline (ND) postoperatively. The study involved 192 patients with left frontal DLGG. MRI data were analyzed to derive whole-brain tumor burden metrics, including tumor radiomics, whole-brain cortical thickness, myelin content, and network characteristics. postoperative inflammatory and molecular markers were collected. Postoperative follow-up neurocognitive function was assessed using the Montreal Cognitive Assessment at 3 months and 1 year. Machine learning models were constructed using Pycaret.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Glioma

Currently open trials in the same condition.

Other West China Hospital trials

Trials by the same sponsor.

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