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Trial Title:
Magnetic Resonance Elastography in Glioma: Exploring Tumor Stiffness and Adhesion
NCT ID:
NCT05990244
Condition:
Glioma
Conditions: Official terms:
Glioma
Conditions: Keywords:
Magnetic Resonance Elastography
Brain tumor
Glioblastoma
MR elastography
Tumor molecular pathology
Study type:
Interventional
Study phase:
N/A
Overall status:
Recruiting
Study design:
Allocation:
N/A
Intervention model:
Single Group Assignment
Primary purpose:
Diagnostic
Masking:
None (Open Label)
Intervention:
Intervention type:
Diagnostic Test
Intervention name:
Magnetic Resonance Elastography
Description:
Undergo MRE and routine MRI
Arm group label:
Diagnostic (MRE, tumor grade, tumor stiffness and adhesion)
Other name:
MRE
Intervention type:
Procedure
Intervention name:
Assessment and Recording
Description:
Undergo recording of tumor stiffness during surgery and molecular pathological
classification through genetic analysis
Arm group label:
Diagnostic (MRE, tumor grade, tumor stiffness and adhesion)
Summary:
this study will investigate the relationship between tumor stiffness and adhesion in
gliomas using MRE. By utilizing preoperative MRE and Intraoperative neuronavigation,
followed by comprehensive molecular pathology analysis, we aim to explore the correlation
of tumor stiffness and adhesion with molecular and genetic characteristics of gliomas.
Additionally, the predictive value of MRE in terms of pathological staging and prognosis
will be determined. This research may pave the way for improved clinical decision-making,
personalized treatment approaches, and more accurate clinical trials for glioma patients.
Detailed description:
Magnetic Resonance Elastography (MRE) is an advanced imaging technique that measures the
mechanical properties of tissues, providing valuable information about tissue stiffness,
elasticity, and adhesion. In the case of gliomas, a type of brain tumor arising from
glial cells, MRE has shown promising potential in the diagnosis, classification, and
prediction of pathological and molecular features.
This clinical trial aims to investigate the relationship between tumor stiffness,
adhesion, glioma grading, and genetic alterations by combining magnetic resonance
elastography (MRE) imaging findings with molecular pathological analysis. Moreover, the
study aims to predict patient survival based on the physical properties of the tumor.
Preoperatively, we will use MRE to enhance the accuracy of navigation and determine tumor
stiffness and adhesion properties. Intraoperatively, under the guidance of
neuronavigation, tissue samples will be obtained, and the operating surgeon will assess
the tumor's stiffness, elasticity, and degree of adhesion.
Postoperatively, all tissue specimens will undergo molecular pathological analysis. The
integration of MRE findings with molecular pathology data will enable precise
classification and subtyping of gliomas.
Furthermore, all patients will receive systematic treatment after surgery, and long-term
follow-ups will be conducted. This comprehensive approach combining MRE, molecular
pathology analysis, and clinical follow-up aims to investigate the predictive value of
MRE in terms of molecular pathological features and prognosis in gliomas.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
- All patients undergoing glioma resection surgery are eligible for inclusion in the
study cohort.
Exclusion Criteria:
- Patients with metallic implants or foreign bodies in their bodies (pacemakers,
artificial metallic heart valves, metal joints, metal implants, and those who cannot
remove dentures, insulin pumps, or contraceptive rings)
- Pregnant women in the first trimester (within three months)
- Patients with severe claustrophobia or anxiety
- Patients with severe fever
- Patients who can not tolerate MRE
- Patients with vascular malformations and aneurysms.
- Patients who do not sign an informed consent
Gender:
All
Minimum age:
18 Years
Maximum age:
80 Years
Healthy volunteers:
Accepts Healthy Volunteers
Locations:
Facility:
Name:
Shengjing Hospital
Address:
City:
Shenyang
Zip:
110000
Country:
China
Status:
Recruiting
Contact:
Last name:
Yu Shi, MD
Phone:
+8618940259980
Email:
18940259980@163.com
Contact backup:
Last name:
Anhua Wu, MD
Phone:
+8618900925766
Email:
wuanhua@yahoo.com
Investigator:
Last name:
Yu Shi, MD
Email:
Principal Investigator
Investigator:
Last name:
Anhua Wu, MD
Email:
Principal Investigator
Investigator:
Last name:
Wen Cheng, MD
Email:
Principal Investigator
Start date:
July 1, 2023
Completion date:
July 1, 2026
Lead sponsor:
Agency:
Shengjing Hospital
Agency class:
Other
Source:
Shengjing Hospital
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05990244