Effect of Deep TMS on the Permeability of the BBB in Patients With Glioblastoma Multiforme: a Pilot Study
Primary Purpose
Glioblastoma Multiforme of Brain
Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Deep Transcranial Magnetic Stimulation (dTMS)
Sponsored by
About this trial
This is an interventional basic science trial for Glioblastoma Multiforme of Brain
Eligibility Criteria
Inclusion Criteria:
- Histological diagnosis of glioblastoma multiforme (WHO grade IV)
- Craniotomy with resection of the tumor at least one year prior to the study
- Treatment with steroids or chemotherapy stable for at least four weeks prior to study enrollment
Exclusion Criteria:
- History of epilepsy
- Presence of cardiac pacemaker
- Presence of neurostimulators
- Presence of surgical clips or medical pumps
- Allergy to contrast medium for Magnetic Resonance Imaging
- History of head injuries
- Alcoholism or drugs abuse
- State of pregnant or breastfeeding
- Severe psychiatric disorders
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Real-Sham dTMS
Sham-Real dTMS
Arm Description
This arm will be treated before with real deep Transcranial Magnetic Stimulation (dTMS) (the first day) and after with sham dTMS (the second day)
This arm will be treated before with sham deep Transcranial Magnetic Stimulation (dTMS) (the first day) and after with real dTMS (the second day)
Outcomes
Primary Outcome Measures
Change in blood-brain barrier permeability
The efficacy of the deep Transcranial Magnetic Stimulation (dTMS) in modulating blood-brain barrier permeability in patients with glioblastoma multiforme through the measurement of the average value of the slope-value distribution function (CDF) evidenced with dynamic contrast-enhanced magnetic resonance imaging
Secondary Outcome Measures
Number of patients with adverse events as a measure of safety and tolerability
To evaluate the safety of the deep Transcranial Magnetic Stimulation (dTMS) applied in patients with glioblastoma multiforme
Full Information
NCT ID
NCT02474966
First Posted
June 11, 2015
Last Updated
June 17, 2015
Sponsor
University of Roma La Sapienza
1. Study Identification
Unique Protocol Identification Number
NCT02474966
Brief Title
Effect of Deep TMS on the Permeability of the BBB in Patients With Glioblastoma Multiforme: a Pilot Study
Official Title
Effects of Deep Transcranial Magnetic Stimulation on the Permeability of the Blood-brain Barrier in Patients With Glioblastoma Multiforme: a Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
June 2015
Overall Recruitment Status
Completed
Study Start Date
November 2014 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
May 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Roma La Sapienza
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The blood-brain barrier (BBB) is a specialized interface allowing a unique environment for neuro-glia networks. BBB dysfunction is common in brain disorders. The Transcranial Magnetic Stimulation (TMS) is a non-invasive method of stimulating cortical motor neurons with the use of rapidly changing electromagnetic fields generated by a coil placed over the scalp. The objective of this study is to evaluate the safety and effects of the deep TMS (dTMS) on barrier integrity in patients with malignant glial tumors. BBB permeability will be quantified using dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI). Permeability change will be compared between two DCE-MRI scans performed immediately after "real" and "sham" rTMS, randomly assigned within one week of each other.
Detailed Description
The blood-brain barrier (BBB) is a specialized interface allowing a unique environment for neuro-glia networks. BBB dysfunction is common in brain disorders. However, the mechanisms underlying BBB opening are poorly understood. The investigators suggest a novel mechanism modulating BBB integrity and therapeutic implications in patients with glioblastoma multiforme. The Transcranial Magnetic Stimulation (TMS) is a noninvasive method of stimulating cortical motor neurons through the scalp and skull capable of inducing electrical currents and depolarizing neurons in focal brain areas with the use of rapidly changing electromagnetic fields generated by a coil placed over the scalp. The objective of this study is to evaluate the safety and effects of the deep TMS (dTMS) on barrier integrity in 20 patients with malignant glial tumors (glioblastoma multiforme). BBB permeability will be quantified using dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI). Permeability change will be compared between two DCE-MRI scans performed immediately after "real" and "sham" dTMS, randomly assigned within one week of each other.
Design of study: Randomized double-blind crossover study. Patients will present on two consecutive days in order to receive dTMS followed by DCE-MRI. Subjects will be randomized into two groups: the first group will be treated before with real-dTMS (the first day) and after with sham-dTMS (the second day); the second group will be treated before with sham-dTMS (the first day) and after with real-dTMS (the second day). At the end of each session of dTMS the patients will undergo by MRI exams.
Enrolled patients: twenty patients with glioblastoma multiforme treated with craniotomy and gross tumor resection or maximal debulking at least a year prior to the study and treated with standard post-operative radiotherapy and adjuvant chemotherapy.
dTMS will be delivered at 1 Hz, on the anterior periphery of the resected tumor bed using the Hesed-coil (H-coil) (Brainsway Ltd., Jerusalem, Israel). Sham stimulation will be delivered with a sham coil placed in the same helmet able to produce similar sounds and scalp sensations.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glioblastoma Multiforme of Brain
7. Study Design
Primary Purpose
Basic Science
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
15 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Real-Sham dTMS
Arm Type
Experimental
Arm Description
This arm will be treated before with real deep Transcranial Magnetic Stimulation (dTMS) (the first day) and after with sham dTMS (the second day)
Arm Title
Sham-Real dTMS
Arm Type
Experimental
Arm Description
This arm will be treated before with sham deep Transcranial Magnetic Stimulation (dTMS) (the first day) and after with real dTMS (the second day)
Intervention Type
Device
Intervention Name(s)
Deep Transcranial Magnetic Stimulation (dTMS)
Intervention Description
Patients will present on two consecutive days in order to receive dTMS followed by dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI). Subjects will be randomized into two groups: the first group will be treated before with real-dTMS (the first day) and after with sham-dTMS (the second day); the second group will be treated before with sham-dTMS (the first day) and after with realTMS (the second day). At the end of each session of dTMS the patients will undergo by MRI exams.
Primary Outcome Measure Information:
Title
Change in blood-brain barrier permeability
Description
The efficacy of the deep Transcranial Magnetic Stimulation (dTMS) in modulating blood-brain barrier permeability in patients with glioblastoma multiforme through the measurement of the average value of the slope-value distribution function (CDF) evidenced with dynamic contrast-enhanced magnetic resonance imaging
Time Frame
Six months
Secondary Outcome Measure Information:
Title
Number of patients with adverse events as a measure of safety and tolerability
Description
To evaluate the safety of the deep Transcranial Magnetic Stimulation (dTMS) applied in patients with glioblastoma multiforme
Time Frame
Six months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Histological diagnosis of glioblastoma multiforme (WHO grade IV)
Craniotomy with resection of the tumor at least one year prior to the study
Treatment with steroids or chemotherapy stable for at least four weeks prior to study enrollment
Exclusion Criteria:
History of epilepsy
Presence of cardiac pacemaker
Presence of neurostimulators
Presence of surgical clips or medical pumps
Allergy to contrast medium for Magnetic Resonance Imaging
History of head injuries
Alcoholism or drugs abuse
State of pregnant or breastfeeding
Severe psychiatric disorders
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maurizio Inghilleri, Professor
Organizational Affiliation
University "Sapienza" of Rome
Official's Role
Principal Investigator
12. IPD Sharing Statement
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Effect of Deep TMS on the Permeability of the BBB in Patients With Glioblastoma Multiforme: a Pilot Study
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