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Glioma, Malignant clinical trials

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NCT ID: NCT05896449 Completed - Glioma, Malignant Clinical Trials

Predictive Values of Preoperative [68Ga]Ga-PSMA-11 PET/CT in Patients With Suspected Brain Tumours of Glial Origin

Start date: June 1, 2020
Phase: N/A
Study type: Interventional

The aim of this study was to analyse usefulness of [68Ga]Ga-PSMA-11 PET/CT scans in preoperative differentiation between HGG and LGG in patients with suspicion of a tumor of glial origin in previously performed imaging examinations. The PET/CT scan will be compared with postoperative histopathological results and with additional immunohistochemical staining for PSMA expression.

NCT ID: NCT05873946 Completed - Glioblastoma Clinical Trials

Assessing the Effectiveness of 2D Non-Navigated Intraoperative Ultrasound in Glioma Surgery

2D-ioUS-Glio
Start date: June 1, 2018
Phase:
Study type: Observational

This retrospective study aims to assess the utility of 2D non-navigated intraoperative ultrasound (ioUS) as a cost-effective alternative for guiding the surgical resection of gliomas and for detecting residual tumor. The study will analyse the records from consecutive adult patients diagnosed with gliomas, undergoing craniotomy between June 2018 and June 2023. The extent of resection (EOR) will be determined using postoperative MRI as the gold standard. The study will also examine the sensitivity and specificity of ioUS in detecting residual tumor. This research seeks to determine if ioUS can be an affordable and reliable tool that, combined with other intraoperative adjuncts, may aid neurosurgeons in achieving the maximum safe resection in glioma surgery.

NCT ID: NCT05806619 Completed - Glioma, Malignant Clinical Trials

Glioma: Biomolecular Aspects

GLIOMA
Start date: October 22, 2019
Phase:
Study type: Observational [Patient Registry]

Main limitations in Glioma studies are due to the wide heterogeneity and genetic instability of the tumor and to the fact that the molecular informations are static, i.e. obtained on the tumor at its onset. Instead, spontaneous or therapy-induced variations are difficult to evaluate and they would need further sampling of the tumor throughout the clinical history. Currently these data are more and more routinely used not only for diagnostics but also in the clinical management of the patient. Furthermore, microenvironment study is becoming increasingly important. It is also important correlate morpho-functional pathway and brain Magnetic Resonance. Therefore, the main goal of the study is to correlate the data obtained with morphological (site, signal intensity, margins, behavior after contrast medium infusion, mismatch between T2 and FLAIR sequences) and non-morphological MR imaging through a radiomic approach and Diffusion and Perfusion study, with molecular data relating to the IDH mutation, MGMT gene promoter methylation, 1p/19q co-deletion and EGFRvIII expression. Furthermore, it is proposed to carry out a correlation between the radiological data and the mutations found in the NGS panel.

NCT ID: NCT05100602 Completed - Glioma, Malignant Clinical Trials

Clinical Evaluation of Genetron TERT PCR Kit in Glioma Patients

Start date: May 13, 2016
Phase:
Study type: Observational

The purpose of this trail is to evaluate the performance of Genetron TERT PCR Kit in Glioma patients using real-time PCR method.

NCT ID: NCT05100173 Completed - Glioma, Malignant Clinical Trials

Clinical Evaluation of Genetron IDH1 PCR Kit in Glioma Patients

Start date: May 13, 2016
Phase:
Study type: Observational

The purpose of this trail is to evaluate the performance of Genetron IDH1 PCR Kit in Glioma patients using real-time PCR method.

NCT ID: NCT04924127 Completed - Glioma, Malignant Clinical Trials

Molecular Pathology Research Project of Glioma

Start date: December 5, 2019
Phase:
Study type: Observational

Evaluate the diagnostic value of TERT promoter mutation in differ glioma subtypes and expend the application of the diagnostic algorithm to surgical practice

NCT ID: NCT04904419 Completed - Glioma, Malignant Clinical Trials

Multi-center Research Project for Glioma Molecular Pathology Intraoperative Rapid Detection

Start date: August 1, 2021
Phase:
Study type: Observational

We explores the accuracy and sensitivity of rapid intraoperative detection of IDH, TERT, BRAF indicators through a prospective clinical multi-center study. This part includes a total of 300 fresh tissue samples, paired blood samples, relevant clinical information and follow-up information from 300 patients with different grades of adult glioma. By comparing with the postoperative sequencing results, the specificity and sensitivity of intraoperative IDH and TERT rapid detection results are clear.

NCT ID: NCT04497142 Completed - Surgery Clinical Trials

Effect of Perampanel on Peritumoral Hyperexcitability in HGG

Start date: November 5, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this research study is to learn more about seizures in people with primary brain tumors. It will evaluate whether an antiseizure medication decreases hyperexcitability activity around tumors and prevents seizures. The procedure and study drug involved in this study are: - Electrocorticography - Perampanel (Fycompa)

NCT ID: NCT04091503 Completed - Gliosarcoma Clinical Trials

Evaluate the Safety and Effectiveness of Intranasal Administration of Temozolomide in Patients With Glioblastoma

Start date: December 20, 2019
Phase: Phase 1
Study type: Interventional

The purpose of this pilot study is to determine the safety, tolerability, and the maximum tolerated dose intranasal administration of temozolomide (TMZ) as a single agent in Treatment on the patients with GBM. Intranasal administration is a new method of treating brain tumours for the direct administration of drugs, inhibitors or viruses, with minimal involvement of the BBB. The investigators know the orally prescribed standard chemotherapy temozolomide (TMZ) is widely used to treat glioma tumours. Received evidence of safety and efficacy in a full cycle of preclinical trials (on GLP Standart) and tests of calculated doses of intranasal administration of TMZ in healthy volunteers. Intranasal administration of temozolomide is considered as GBM therapy, which provides direct access to a therapeutic dose of the drug into the brain (to the neoplastic process) with low toxicity