Low Frequency Electrical Stimulation of the Fornix in Intractable Mesial Temporal Lobe Epilepsy (MTLE)

Not Applicable

Completed

Conditions: Mesial Temporal Lobe Epilepsy

Interventions: Device: Medtronic Deep Brain Stimulation

Registration Number: NCT02383407

Lead Sponsor: George Washington University

Brief Summary: The primary aim of the current proposal is to evaluate safety and tolerability, in terms of neuropsychological effects of low frequency electrical stimulation of the fornix (LFSF) in participants with medically-intractable Mesial Temporal Lobe Epilepsy. Secondary aims include evaluation of psychiatric changes, seizure frequency, and quality of life during LFSF.

Detailed Description: Low frequency stimulation is an attractive, uninvestigated method for treatment of intractable epilepsy. Preliminary animal and human data suggest safety and remarkable efficacy of Low frequency stimulation (LFS) in epilepsy. In addition, the duty cycle of LFS is very low, implying less electric current injection, with less charge density on the target tissue and electrodes, and longer battery life. The current project is a classic translational, single-blinded, randomized research project, demonstrating a clear path from the laboratory to bedside. If successful, this new therapy will be of great value to patients with medically and surgically intractable Mesial Temporal Lobe Epilepsy (MTLE).

The study is expected to last approximately 5 years, from enrollment of the first patient to completion of the final subject, taking into consideration attrition and otherwise-eligible subjects who will not elect to participate. Once the study is completed, and enrolled participants have completed all required elements of the protocol, a final report will be submitted to the FDA. Participants may also discontinue their participation in the study, if they wish, at any time.

Recruitment & Eligibility

Status: COMPLETED

Sex: All

Target Recruitment: 6

Inclusion Criteria

Participants are between the ages of 18 -65 years of age
Participants must have had a non-invasive video-EEG monitoring revealing seizure semiology and ictal EEG consistent with unilateral or bilateral MTLE
Participants must have tried and failed two trials of antiepileptic drugs (AEDs)
Participants may have lesional or non lesional hippocampi, as evidenced by brain MRI acquired within the previous two years
Participants are prescribed and taking 1-4 AEDs at the time of study entry
Study participants will have intractable (MTLE) with a seizure frequency of at least 1/month averaged over the preceding 6 months prior to enrollment, including maximum seizure-freedom periods of no more than 60 days.
Participants must have a platelet count greater than 125,000 per cubic millimeter and prothrombin time (PT) and activated partial thromboplastin time (aPTT) within normal limits at the visit prior to surgery

Exclusion Criteria

Progressive neurological or medical diseases, such as brain tumors or neurodegenerative disease or cancer
Non-compliance with antiepileptic medications as demonstrated by the medical record
Any conditions interfering with electrode implantation
Any non-epileptic seizures
Inability or unwillingness to complete neuropsychological tests or complete seizure diaries
Current drug or alcohol use or dependence that, in the opinion of the site investigator, would interfere with adherence to study requirements
Pregnant, or planning to become pregnant*
Participation in another research trial where the participant was treated with another investigational drug or device within 30 days prior to enrollment of study
Intelligence Quotient showing a general ability Quotient of less than 70. The score excludes the contribution of working memory and processing speed (which are areas of cognitive functioning that are vulnerable to numerous influences including seizures and fatigue and effects of AEDs)
Inability or unwillingness of individual to give written informed consent
Participants who have changes to their antiepileptic medications during the baseline phase (as they will need to repeat the baseline phase)
Subjects with history of status epilepticus within the preceding year
History of psychiatric illness necessitating hospitalizations
Subjects who have any of the following implanted devices: aneurysm clips, cardiac pacemaker or defibrillator, cochlear implant, spinal cord, DBS, or vagal nerve stimulator
Co-morbid conditions that would interfere with study stimulation activities or response to treatment, which may include:
- Neoplasm with life expectancy < 5 years
- Severe chronic pulmonary disease
- Local, systemic acute or chronic infectious illness
- Life threatening cardiac arrhythmias
- Severe collagen vascular disorder
- Kidney failure or other major organ system failures

Study & Design

Study Type: INTERVENTIONAL

Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Stimulation group 5 Hz	Medtronic Deep Brain Stimulation	Patient will be randomized to a stimulation group of 5 Hz using Medtronic deep brain stimulation device
Stimulation group 2 Hz	Medtronic Deep Brain Stimulation	Patient will be randomized to a stimulation group of 2 Hz using Medtronic deep brain stimulation device

Primary Outcome Measures

Name	Time	Method
Safety and Tolerability of Low Frequency Stimulation of the Fornix With Regards to Memory Function	1 year	The primary outcome is safety and tolerability of LFSF in participants with intractable MTLE with regards to memory function. The number of participants listed are those who had a significant changes in RAVLT score.

Secondary Outcome Measures

Name	Time	Method
To Assess if Electrode Implantation in the Fornix is Feasible as is Done in Patients With Parkinson's Disease.	1 year	The DBS leads are routinely implanted for patients with Parkinson's disease. Thus, we planned to implant Model 3389 DBS leads using the same technique of stereotactic implantation. A secondary aim of this trial is to standardize the implantation, the evoked potential and electric current determination procedures in preparation for a large-scale phase III trial. The number of participants with the outcome measure are those in whom bilateral hippocampal CCEPs were consistently present.
Psychiatric Health (Effects of LFS on Psychiatric Symptoms Using Standardized Measures That Are Known to be Sensitive to Changes to Surgical Treatment of TLE)	1 year	Since LFSF is expected to activate limbic structures, we will assess the effects of LFS on psychiatric symptoms using standardized measures that are known to be sensitive to changes to surgical treatment of TLE. The number of participation listed are those who had a significant change in anxiety, depression, or suicidality based on a qualitative overview of the psychiatric assessments performed preoperatively and postoperatively.
Effect on Seizure Frequency	1 year	Seizure reduction: Subjects underwent implantation of pulse generators and long-term low-frequency stimulation with mean monthly seizures during blinded phase