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Fluorescein vs. iMRI in Resection of Malignant High Grade Glioma

Fluorescein vs. Intraoperative MRI in the Resection of Malignant High Grade Glioma

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02540135
Enrollment
0
Registered
2015-09-03
Start date
2015-03-01
Completion date
2018-07-18
Last updated
2018-07-20

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

Conditions

High Grade Malignant Neoplasm, Glioblastoma Multiforme, Anaplastic Astrocytoma

Keywords

high grade glioma, glioblastoma multiforme, anaplastic astrocytoma, flourescein, flourescence-guided surgery, intraoperative MRI, iMRI

Brief summary

This study plans to learn more about if fluorescein with intraoperative Magnetic Resonance Imaging (MRI) is as good as intraoperative MRI (iMRI) alone in detecting the presence of tumor tissue during surgery. Both fluorescein and intraoperative MRI have been studied and routinely used to aid the neurosurgeon in distinguishing normal brain from tumor, helping the neurosurgeon to safely resect more tumor tissue during surgery. This study will enroll patients with malignant high grade glioma who are going to have a surgery to remove their brain tumor. For half of the patients, fluorescein and intraoperative MRI will be used together during surgery. For half of the patients, only intraoperative MRI will be used during surgery. iMRI is used as final verification of complete, safe resection in both arms.

Detailed description

Extent of surgical resection of malignant high grade glioma has been established as one of the most important predictors of overall survival and six-month progression free survival. Unfortunately, it is often difficult in surgery to distinguish between tumor and normal brain. Various technologies have been developed to help the surgeon more readily safely increase extent of resection in order to achieve an improved survival after glioblastoma resection. Fluorescein has been used at some institutions for a number of years to improve visualization of high-grade gliomas enabling their better resection. Intraoperative MRI has also been developed with similar intent, allowing the patient to be imaged intraoperatively to determine extent of resection and any need for further resection prior to leaving the operating room. While there is some evidence these technologies improve extent of resection in comparison to historical controls, they have never been tested against each other in any prospective fashion. Intraoperative MRI has significant cost and significantly increases operative time. Fluorescein is a very inexpensive injectable agent and, if as good at achieving gross total resection as intraoperative MRI, would offer patients similar surgical outcomes with less anesthetic time and cost than intraoperative MRI. This study aims to investigate the value of fluorescein or intraoperative MRI in malignant glioma patients' extent of tumor resection in a prospectively randomized manner.

Interventions

fluorescein and conventional neuro-navigation

conventional neuro-navigation and iMRI

Sponsors

University of Colorado, Denver
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Eligibility

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

Inclusion criteria

* Presents with presumed or pathologically proven enhancing primary or secondary high grade glioma for surgical resection * Eligible for gross total resection of enhancing component of tumor * Karnofsy performance status \>/= 70%

Exclusion criteria

* Presence of multi-focal disease * Disease that crosses the mid-line * History of adverse reaction to flourescein * Known ongoing pregnancy * Inability to grant consent * Contraindication to perform iMRI * Contraindication to flourescein

Design outcomes

Primary

MeasureTime frameDescription
Extent of resection36 hoursThis outcome will utilize tumor volumetry of residual enhancing tumor after resection.

Secondary

MeasureTime frameDescription
Surgical time difference36 hoursThis outcome will evaluate the difference in length of surgery time between each arm.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026