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MRI-Guided Focused Ultrasound Feasibility Study for Brain Tumors

Primary Purpose

Brain Tumor

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ExAblate transcranial system
Sponsored by
InSightec
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Brain Tumor focused on measuring Brain tumor, Brain Lesions, Brain Cancer, ExAblate

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Men or women. Age between 18 and 70 years, inclusive. Able and willing to give informed consent. Subjects with (newly diagnosed or recurrent) metastatic cancer for whom surgery, radiation, or radiosurgery has not been advised by the treating physician. The targeted tumor tissue is located in the cerebral hemispheres, > 2.5 cm from the inner table of the skull. Non-targeted parts of the tumor may extend outside the treated tumor limits. Tumor(s) are clearly defined on pre-therapy contrast enhanced MRI scans. Size of the targeted portion of the tumor (i.e. prescribed Region Of Treatment) is less than 2.5 cm in diameter or 8 cm3 in volume. The non-targeted tumor tissue may exceed the targeted volume. Karnofsky rating 70-100 (See Appendix A). ASA score 1-2. Able to communicate sensations during the ExAblate MRGFUS procedure. Able to attend all study visits (i.e. life expectancy of at least 3 months). At least 14 days passed since last brain surgery, or intracranial radiation therapy/radiosurgery Exclusion Criteria: The subject presents with: - Symptoms and signs of increased intracranial pressure (e.g., headache, nausea, vomiting, lethargy, and papaedema). - Unstable hemodynamic status including: i. Documented myocardial infarction within six months of enrollment. ii.Symptomatic coronary artery stenosis. iii. Congestive heart disease requiring medication. iv. Anti-arrhythmic drug medication. v. Cardiac pacemaker. vi. Severe hypertension (diastolic BP > 100 on medication). Anti-coagulant therapy, on medications known to increase risk of hemorrhage, (e.g.: non-steroidal anti-inflammatory drugs (NSAIDs), statins TIA or stroke in the last 1 month Insulin-dependent diabetes mellitus Immunosuppression (corticosteroids to prevent brain edema are permitted) Known sensitivity to gadolinium-DTPA Contraindications to MRI such as non-MRI-compatible implanted devices Large subjects not fitting comfortably into the MRI scanner Difficulty laying supine and still for up to 4 hours in the MRI unit or claustrophobia Untreated, uncontrolled Sleep apnea Positive pregnancy test (for pre-menopausal women) Known life-threatening systemic disease More than 3 metastatic tumors History of abnormal bleeding and coagulopathy Use of Avastin in the preceding two weeks or planned use in the forthcoming two weeks and VEGF inhibitors within + 30 days of treatment Patients with a history of uncontrolled seizures or who are not on anti seizure medication (e.g., Phenytoin 100 mg PO t.i.d. or Keppra 500 mg po bid) before the procedure

Sites / Locations

  • Brigham and Women's Hospital
  • Swedish Medical Center

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

ExAblate transcranial system

Arm Description

MR Guided Focused Ultrasound

Outcomes

Primary Outcome Measures

Number of subjects with Serious and Non-Serious Adverse Events after MRI Guided Focused ultrasound treatment for brain tumors
To evaluate the safety of ExAblate TcMRgFUS treatment delivered through intact human skull to the brain, during the treatment and during the follow-up period of 3 months.

Secondary Outcome Measures

Full Information

First Posted
September 2, 2005
Last Updated
September 7, 2021
Sponsor
InSightec
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1. Study Identification

Unique Protocol Identification Number
NCT00147056
Brief Title
MRI-Guided Focused Ultrasound Feasibility Study for Brain Tumors
Official Title
A Study to Evaluate the Safety and Feasibility of Transcranial MRI-Guided Focused Ultrasound Surgery in the Treatment of Brain Tumors
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Unknown status
Study Start Date
August 2012 (undefined)
Primary Completion Date
December 2022 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
InSightec

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to evaluate the safety of MRI-guided focused ultrasound thermal ablation of brain tumors performed through intact human skull using the ExAblate transcranial system. We will collect data to establish the basic safety of this type of treatment as the basis for later studies that will evaluate its clinical efficacy.
Detailed Description
In this non-randomized feasibility study, FUS under MRI-guidance and thermometry will be given through intact human skull to brain tumor in up to ten (10) subjects. These subjects will be followed over a 3-month period with contrast MRI and clinical exams. The objectives are: To evaluate the safety of ExAblate TcMRgFUS treatment delivered through intact human skull to the brain, during the treatment, and during the follow-up period of 3 months. To evaluate the effect of thermal ablation in the target tumor with contrast MR imaging to identify viable tumor, and non-viable thermally ablated tissue.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Brain Tumor
Keywords
Brain tumor, Brain Lesions, Brain Cancer, ExAblate

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
ExAblate transcranial system
Arm Type
Experimental
Arm Description
MR Guided Focused Ultrasound
Intervention Type
Device
Intervention Name(s)
ExAblate transcranial system
Intervention Description
MRI-Guided Focused Ultrasound Feasibility Study for Brain
Primary Outcome Measure Information:
Title
Number of subjects with Serious and Non-Serious Adverse Events after MRI Guided Focused ultrasound treatment for brain tumors
Description
To evaluate the safety of ExAblate TcMRgFUS treatment delivered through intact human skull to the brain, during the treatment and during the follow-up period of 3 months.
Time Frame
Up to 3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men or women. Age between 18 and 70 years, inclusive. Able and willing to give informed consent. Subjects with (newly diagnosed or recurrent) metastatic cancer for whom surgery, radiation, or radiosurgery has not been advised by the treating physician. The targeted tumor tissue is located in the cerebral hemispheres, > 2.5 cm from the inner table of the skull. Non-targeted parts of the tumor may extend outside the treated tumor limits. Tumor(s) are clearly defined on pre-therapy contrast enhanced MRI scans. Size of the targeted portion of the tumor (i.e. prescribed Region Of Treatment) is less than 2.5 cm in diameter or 8 cm3 in volume. The non-targeted tumor tissue may exceed the targeted volume. Karnofsky rating 70-100 (See Appendix A). ASA score 1-2. Able to communicate sensations during the ExAblate MRGFUS procedure. Able to attend all study visits (i.e. life expectancy of at least 3 months). At least 14 days passed since last brain surgery, or intracranial radiation therapy/radiosurgery Exclusion Criteria: The subject presents with: - Symptoms and signs of increased intracranial pressure (e.g., headache, nausea, vomiting, lethargy, and papaedema). - Unstable hemodynamic status including: i. Documented myocardial infarction within six months of enrollment. ii.Symptomatic coronary artery stenosis. iii. Congestive heart disease requiring medication. iv. Anti-arrhythmic drug medication. v. Cardiac pacemaker. vi. Severe hypertension (diastolic BP > 100 on medication). Anti-coagulant therapy, on medications known to increase risk of hemorrhage, (e.g.: non-steroidal anti-inflammatory drugs (NSAIDs), statins TIA or stroke in the last 1 month Insulin-dependent diabetes mellitus Immunosuppression (corticosteroids to prevent brain edema are permitted) Known sensitivity to gadolinium-DTPA Contraindications to MRI such as non-MRI-compatible implanted devices Large subjects not fitting comfortably into the MRI scanner Difficulty laying supine and still for up to 4 hours in the MRI unit or claustrophobia Untreated, uncontrolled Sleep apnea Positive pregnancy test (for pre-menopausal women) Known life-threatening systemic disease More than 3 metastatic tumors History of abnormal bleeding and coagulopathy Use of Avastin in the preceding two weeks or planned use in the forthcoming two weeks and VEGF inhibitors within + 30 days of treatment Patients with a history of uncontrolled seizures or who are not on anti seizure medication (e.g., Phenytoin 100 mg PO t.i.d. or Keppra 500 mg po bid) before the procedure
Facility Information:
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
Swedish Medical Center
City
Seattle
State/Province
Washington
ZIP/Postal Code
98122
Country
United States

12. IPD Sharing Statement

Links:
URL
http://www.insightec.com
Description
Sponsor web page

Learn more about this trial

MRI-Guided Focused Ultrasound Feasibility Study for Brain Tumors

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