Evaluation of the Brain Activity During Spinal Cord Stimulation in Failed Back Surgery Syndrome Using Functional MRI and MRS
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Purpose
Functional Magnetic Resonance Imaging (fMRI)and MR Spectroscopy of the brain are perfect tools to investigate the changes in the brainstem and brain evoked by the orthodromically impulses of a SCS.
| Condition | Intervention |
|---|---|
|
Failed Back Surgery Syndrome |
Other: fMRI and MRS |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Basic Science |
| Official Title: | Evaluation of the Brain Activity During Spinal Cord Stimulation (SCS) in Failed Back Surgery Syndrome Using Functional Magnetic Resonance Imaging (fMRI) and Magnetic ResonanceSpectroscopy (MRS) |
- functional and neurobiological cerebral changes due to SCS [ Time Frame: 2 years ] [ Designated as safety issue: No ]To compare brain activity before and after spinal cord stimulation (with appropriate paraesthesia) using functional magnetic resonance imaging and neurobiological changes in the spectrum (gamma-aminobutyric acid (GABA) glutamate (Glu) glutamine (Gln) N-acetylaspartate (NAA) Choline-containing compounds (Cho) Creatine plus phophocreatine (total creatine: Cr) Myo-inositiol (Ins) Choline (Cho) Glucose (Glc) Lactate (Lac)) due to stimulation measured by MRS. The primary outcome is the difference in neurobiology between baseline and when the stimulator is on.
| Estimated Enrollment: | 40 |
| Study Start Date: | September 2008 |
| Estimated Study Completion Date: | September 2011 |
| Estimated Primary Completion Date: | September 2010 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
SCS
patients with Failed back Surgery syndrome treated with SCS
|
Other: fMRI and MRS
fMRI and MRS
|
Detailed Description:
In case a patient meets all inclusion and no exclusion criteria, he/she will be implanted with an epidural neurostimulation lead (electrode).
The day of implant will be recorded as day 0 (table 1) and will always be a Thursday.
Post lead implant, the patient will be hospitalized for a small week as per common practice in case of the intervention outside of the study.
During hospital stay, the investigator of the study, or a representative of the product manufacturer, Medtronic®, will search for the optimal stimulation parameters to evoke correct paraesthesia coverage and pain relief. If appropriate parameters have been found, these will be saved in the external neurostimulator.
After maximum one hour, the neurostimulator will be turned off again.
On day 12, a Tuesday, a MR spectrospoy will be performed. Each patient will undergo three sessions.
Each session will be divided into a MR spectroscopy session and fMRI session without stimulation and a session with stimulation. The MR spectroscopy session without stimulation will bring us the baseline in neurobiology of neuropathic pain; after measurement, the stimulator will be switch on and a MR spectroscopy will be performed during a longer period of time (10 min) in order to determine neurobiological changes in time during SCS.
The 3 MR spectroscopy sessions will be performed on different regions in the brain (both talami and rostral region of anterior cingulated cortex)
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Age male/female patient ≥ 18 years
- Patient diagnosed with Failed Back Surgery Syndrome with at least one prior spinal surgery
- Patient with low back pain and/or pain in at least one leg
- Pain intensity at baseline assessed by VAS > 5 (50%)
- Patient willing to provide informed consent.
Exclusion Criteria:
- Use of spinal cord stimulation in this patient in the past.
- Presence of other clinically significant or disabling chronic pain condition
- Expected inability of patients to receive or properly operate the spinal cord stimulation system
- History of coagulation disorders, lupus erythematosus, diabetic neuropathy, rheumatoid arthritis or morbus Bechterew
- Active malignancy
- Current use of medication affecting coagulation which cannot be temporarily stopped
- Evidence of an active disruptive psychiatric disorder or other known condition significant enough to impact perception of pain, compliance to intervention and/or ability to evaluate treatment outcome as determined by investigator
- Life expectancy of less than 1 year
- Existing or planned pregnancy
- Existing extreme fear for entering MRI
Contacts and Locations| Contact: Maarten Moens, MD | 0032478884047 | mtmoens@gmail.com |
| Belgium | |
| UZ Brussel | Recruiting |
| Brussel, Belgium, 1090 | |
| Contact: Maarten Moens, m 0032478884047 mtmoens@gmail.com | |
| Principal Investigator: Maarten Moens, MD | |
More Information
No publications provided
| Responsible Party: | Maarten Moens, MD, Neurosurgery |
| ClinicalTrials.gov Identifier: | NCT01181817 History of Changes |
| Other Study ID Numbers: | vubmtmoensSCS |
| Study First Received: | August 10, 2010 |
| Last Updated: | August 17, 2010 |
| Health Authority: | belgium: Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten |
Keywords provided by Universitair Ziekenhuis Brussel:
|
FBSS at least one prior spinal surgery |
Additional relevant MeSH terms:
|
Failed Back Surgery Syndrome Back Pain Pain Neurologic Manifestations |
Nervous System Diseases Postoperative Complications Pathologic Processes |
ClinicalTrials.gov processed this record on May 16, 2013