Magnetic Resonance Fingerprinting Guided Extended Resection in Glioblastomas
Launched by CASE COMPREHENSIVE CANCER CENTER · Jun 7, 2024
Trial Information
Current as of July 23, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial, titled "Magnetic Resonance Fingerprinting Guided Extended Resection in Glioblastomas," is exploring a new imaging technique called MR fingerprinting. This technique aims to improve the way doctors can see and understand how glioblastomas, which are aggressive brain tumors, spread within the brain. By using MR fingerprinting instead of standard MRI images, the researchers hope to get clearer and more detailed pictures that can help in planning surgery for patients with these tumors.
To participate in this trial, individuals must be over 18 years old and have imaging results that suggest the presence of a glioblastoma with a tumor size larger than 3 cm. They also need to be able to provide written consent and undergo an MRI scan. However, people who have certain conditions that prevent them from having an MRI or surgery, or who have previously been treated for glioblastoma, will not be eligible. If selected, participants can expect to undergo MRI scans to help guide their treatment and potentially improve the outcomes of their surgery. This trial is not yet recruiting participants, but it represents an important step towards improving care for those affected by glioblastoma.
Gender
ALL
Eligibility criteria
- Stage I:
- Inclusion criteria:
- • Age \> 18
- • MR imaging findings suggestive of GB
- • Maximal tumor diameter greater than 3 cm
- • Ability to provide written informed consent
- • Ability to undergo MRI scan
- • Consideration for biopsy, subtotal or gross total resection.
- Exclusion Criteria:
- • Contraindications to MRI
- • Contraindication to surgical treatment
- • Prior treatment for glioblastoma
- Stage II:
- Inclusion Criteria:
- • Age \> 18
- • MR imaging findings suggestive of GB
- • Maximal tumor diameter greater than 3 cm
- • Ability to provide written informed consent
- • Ability to undergo MRI scan
- • Lesions amenable to gross total resection
- • Presence of peritumoral FLAIR signal abnormality beyond the area of enhancement.
- Exclusion Criteria:
- • Inability to undergo MRI imaging
- • Participants undergoing only stereotactic biopsy or less than gross total resection
- • Participants undergoing LITT
- • Inability to consent for the study
- • Previously treated/ recurrent glioma.
About Case Comprehensive Cancer Center
Case Comprehensive Cancer Center is a leading academic research institution dedicated to advancing cancer care through innovative clinical trials and cutting-edge research. As a National Cancer Institute-designated Comprehensive Cancer Center, it integrates multidisciplinary approaches to cancer prevention, diagnosis, and treatment, fostering collaboration among clinicians, researchers, and patients. The center is committed to translating scientific discoveries into effective therapies, enhancing patient outcomes, and contributing to the global body of cancer knowledge. With a robust portfolio of clinical trials, Case Comprehensive Cancer Center aims to address the unmet needs of cancer patients and drive progress in the fight against cancer.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Cleveland, Ohio, United States
Patients applied
Trial Officials
Chaitra Badve, MD
Principal Investigator
University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center
Tiffany Hodges, MD
Principal Investigator
University Hospitals Cleveland Medical Center, Case Comprehensive Cancer Center
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported