A Multicenter Study of Hippocampal Electrical Stimulation (HS, in Mesial Temporal Lobe Epilepsy (METTLE)

University of Calgary

Status and phase

Terminated

Phase 3

Conditions

Temporal Lobe Epilepsy

Treatments

Procedure: Hippocampal Electrical Stimulation

Study type

Interventional

Funder types

Other

Identifiers

NCT00717431

20492

Details and patient eligibility

About

The primary goal is to determine whether hippocampal electrical stimulation (HS) is safe and more effective than simply implanting an electrode in the hippocampus without electrical stimulation (HI), in patients with mesial temporal lobe epilepsy (MTLE). This will be assessed by the rate of complex partial seizures per person-month over 6 months of follow-up in HS vs. HI. There are two treatment arms: 1) Hippocampal Electrode Implantation with Stimulation (HS). 2) Hippocampal Electrode Implantation without stimulation (HI). The investigators expect to demonstrate that HS is safe and superior to HI in controlling seizures in patients with MTLE.

Full description

This is a multicentre, parallel-group, double blind randomized controlled trial involving patients with MTLE who may be candidates for resective surgery or whose memory function precludes resective surgery. Eligible patients will be randomized in a 2:1 ratio into hippocampal electrode implantation with stimulation (HS), or hippocampal electrode implantation without stimulation (HI). Patients will be followed for seven months after randomization. One month will be devoted to adjustment of interventions, and 6 months to follow-up and outcome assessment. At the end of seven months, all patients will be offered the option of HS, electrode removal, surgical therapy or medical therapy, based on best evidence and patient preference.

Primary Question: In patients with MTLE, over a 6-month period:

Is continuous HS plus medical therapy (MT) more efficacious than hippocampal implantation (HI) plus MT in reducing seizure frequency?

Secondary Questions: In patients with MTLE, over a 6-month period:

Is HS safe?
What is the effect of HS on cognition, mood, and quality of life?
What is the effect of HS on psychiatric morbidity?
Is the efficacy of HS associated with the presence, location and amount of interictal hippocampal spikes on depth electrode recordings?

Enrollment

8 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Unilateral or Bilateral Mesial Temporal lobe Epilepsy.
Age ≥ 18 years.
Global IQ ≥70.
Failure of ≥ 2 AEDs approved for treatment of partial seizures, used alone or in combination at recommended dosages.
Average ≥ 3 seizure-days per month in prior 6 months during which disabling seizures occurred. Disabling seizures are defined as complex partial seizures with or without secondary generalization, or as simple partial seizures that are noticeable by others or interfere with function.
Ability to complete self-administered questionnaires.
Availability of reliable collateral historian or witness.
Patient preference for non-resective surgery, or not a candidate for mesial temporal resection.
Give written informed consent.

Exclusion criteria

Extratemporal or multifocal epilepsy.
MRI evidence of potentially epileptogenic lesions outside the mesial temporal region.
Lesions precluding electrode implantation (eg, vascular malformations, vascular tumors).
Severe hippocampal sclerosis that in the surgeon's opinion precludes accurate electrode placement.
Brain lesions that demand prompt surgical therapy (eg, malignant tumors, vascular malformations).
Progressive neurological disorders (eg, malignant tumor, dementia, degenerative disorders).
Medical or psychiatric conditions precluding surgery or interfering with adherence to treatment and follow-up.
Planned pregnancy during the study. Women of child-bearing age will require a negative pregnancy test and adequate contraception methods.
Ongoing or planned participation in other studies of new epilepsy therapies.
Contraindication for stereotactic surgery, e.g. bleeding diathesis, anticoagulants, treatment with valproate at the time of surgery (risk of bleeding).
Any condition that would make participation in the trial detrimental to the patient's health.