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GliomaAI-GBM: MRI-Based Detection of IDH Wildtype Glioblastoma

GliomaAI-GBM: Non-Invasive MRI-Based Detection of IDH Wildtype Glioblastoma Using Artificial Intelligence

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07673692
Acronym
GliomaAI-GBM
Enrollment
1372
Registered
2026-06-29
Start date
2017-03-14
Completion date
2021-07-16
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Glioblastom WHO Grade 4, Glioma, Glioma (Diagnosis), IDH Wildtype Glioblastoma

Keywords

Glioma, Brain Tumour, Glioma AI, MRI, Histological Glioblastoma, IDH Wildtype Glioblastoma

Brief summary

The goal of this observational study is to learn whether an artificial intelligence system called GliomaAI-GBM can help detect a specific molecular type of brain tumour called IDH wildtype glioblastoma using routine MRI scans. The study uses previously collected and fully anonymised MRI data from 1,372 patients from 13 institutions in the Cancer Imaging Archive (TCIA). The main questions it aims to answer are: * How accurately can GliomaAI-GBM identify IDH wildtype glioblastoma from MRI scans? * How well does the system perform across data from different hospitals and patient groups? Researchers will use existing MRI scans and clinical information to train and test the AI system. No new scans, treatments, or hospital visits are required for participants, and all data used is fully anonymised and obtained from an existing research database. Participants will not be asked to do anything, as this study only uses previously collected imaging data.

Interventions

DEVICEGliomaAI-GBM

Software as Medical Device (SaMD) for predicting histological glioblastoma

Sponsors

Deep Learning Institute of Radiological Sciences
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult (\>=18 years of age) * Having pre op MRI scan * Having biopsy / surgery * Having post biopsy/ surgery histology diagnosis and genetic analysis.

Exclusion criteria

* MRI scan significantly degraded by motion or other artefact * Incomplete genetic analysis * Prior treatment (e.g., radiotherapy or chemotherapy) before baseline MRI

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic performance of GliomaAI-GBM for identification of IDH wildtype glioblastoma from MRI, measured by accuracy, sensitivity, specificity, positive predictive value, negative predictive value, and area under the ROC.PerioperativeThe diagnostic performance of the GliomaAI-GBM artificial intelligence model will be assessed by comparing pre-operative MRI-based predictions of IDH wildtype glioblastoma status against post-operative (biopsy or surgery) molecular/genetic profiling results as the reference standard. Performance metrics including accuracy, sensitivity, specificity, positive predictive value, negative predictive value, and AUC will be calculated.

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 30, 2026