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Recruiting Observational

MR Based Prediction of Molecular Pathology in Glioma Using Artificial Intelligence

NCT04217018 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2017-01-01
Last updated
2021-02-08

Condition(s) studied

Glioma

Investigational drug(s) / intervention(s)

Prediction of molecular pathology

Prediction of molecular pathology: Prediction of 1p/19q co-deletion, MGMT methylation, IDH and TERTp mutations or molecular subgroups by leveraging AI

Study summary

This registry aims to collect clinical, molecular and radiologic data including detailed clinical parameters, molecular pathology (1p/19q co-deletion, MGMT methylation, IDH and TERTp mutations, etc) and conventional/advanced/new MR sequences (T1, T1c, T2, FLAIR, ADC, DTI, PWI, etc) of patients with primary gliomas. By leveraging artificial intelligence, this registry will seek to construct and refine algorithms that able to predict molecular pathology or subgroups of gliomas.

Eligibility

Sex
ALL
Min age
1 Year
Max age
95 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Patients must have radiologically and histologically confirmed diagnosis of primary glioma * Life expectancy of greater than 3 months * Must receive tumor resection * Signed informed consent Exclusion Criteria: * No gliomas * No sufficient amount of tumor tissues for detection of molecular pathology * Patients who have any type of bioimplant activated by mechanical, electronic, or magnetic devices * Patients who are pregnant or breast feeding * Patients who are suffered from severe systematic malfunctions

Primary outcome measure(s)

  • AUC of prediction performance — up to 10 years
    AUC=sensitivity+specificity-1

Trial sites (1)

FacilityCityRegionStatus
Department of Neurosurgery, First Affiliated Hospital of Zhengzhou University Zhengzhou Henan Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04217018 on ClinicalTrials.gov ↗ ← All trials in China