A Controlled Clinical Trial of Cathodal Transcranial Direct Current Stimulation in Patients With Refractory Epilepsy

Phase 2

Completed

• Conditions: Refractory Epilepsy

• Registration Number: NCT01763294
• Lead Sponsor: El Instituto Nacional de Neurologia y Neurocirugia Manuel Velasco Suarez

Brief Summary

There is a continuous necessity for the search of new alternatives for safe, affordable and effective noninvasive therapies for patients that are not eligible for focal resective or palliative surgery. The transcranial direct current stimulation (tDCS) therapy has demonstrated to be safe, noninvasive, simple and effective with promising results in case series, case reports and animals models for the treatment of intractable epilepsy. tDCS is a feasible and low cost method to modify cortical excitability in a non-invasive procedure. Its effects on cortical excitability seem to be similar to the effects induced by repetitive transcranial magnetic stimulation. The aim of this study is determine the safety and efficacy in the reduction of the number of seizures (\>50%) and epileptiform activity in patients with refractory and multifocal epilepsy after different protocols of tDCS compared with placebo.

Detailed Description

This is a prospective interventional clinical study. All enrolled patients have multifocal and refractory epilepsy that voluntarily will accept to participate in the study signing a consent informed form. All patients are from the epilepsy clinic our Institute that meet the criteria. All patients will be randomized and divided in 5 groups (45 patients); placebo group, active group of one session 30 minutes, active group of one session of 60 minutes, active group of 30 minutes for 3 consecutively days and 30 minutes for 5 consecutively days. After the selection, the patients will record their EEG of 30 min in order to register the basal epileptic activity and determine the most epileptic area, where the intervention will be applied. Then, an EEG will be realized after the intervention, one month after and two months after.

The equipment used to apply the therapy is approved for medical use in our country. The equipment is Nicolet, Endeavor used at low amplitude for direct electrical nervous stimulation mode. The intensity to apply will be 2 milliampere. The stimulation mode is continuous with frequency of 3 Hz. The site of application depends on the basal EEG findings, nevertheless, it is ruled by the international EEG 10/20 system.

The cathodal electrode is applies with disposable needle of 12 mm long and 0.5 mm wide, while the anodal electrode is applied with conventional cup electrodes with a 2mm hole in the center an a recording surface of silver chloride /silver. After the intervention the patient is asked about any adverse effect form the therapy application and the EEG is realized as the investigators described before. The patient will receive a follow up dates at one and two months. The patient must make a calendar with the frequency of seizures and must not change the actual medication.

Placebo. This group receives the same procedures just that in this case the machine produces a 60 second stimulus at the beginning so the patient can feel the initial electric stimulus.

The investigators will record the frequency of the seizures and analysis of the epileptiform activity in the EEGs in the baseline, after therapy, 1 month and 2 months of follow-up. As well the safety profile of the tDCS.

Study Timeline

• Study Start: 2012-02
• Primary Completion: 2012-12
• Study First Submitted: 2013-01-02
• Study First Submitted QC: 2013-01-05
• Study First Posted: 2013-01-08
• Status Verified: 2015-04
• Study Completion: 2015-04
• Last Update Submitted: 2015-04-05
• Last Update Posted: 2015-04-07

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 28

Inclusion Criteria

• any gender
• age ≥ 15 and <65 years
• Refractory epilepsy characterized by 3 or more seizures by month and the right use of 2 or more antiepileptic drugs during the last 12 months
• Not eligible for surgery treatment
• Right attachment to the antiepileptic treatment established at least 12 months before the date of inclusion
• Multifocal epilepsy defined as 2 or more lobar regions affected with epileptic activity

Exclusion Criteria

• Patients with pseudoseizures
• Previous craniotomy
• Active local infection of the skull
• Informed consent not signed
• Patients with generalized idiopathic epilepsy or focal idiopathic epilepsy
• Patients in stupor or coma
• Patients in lactation or pregnancy
• Patients with chronic degenerative diseases of the nervous system
• Patients with exacerbated chronic degenerative diseases

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Number of seizures	2 months	The number of the seizures monthly for 2 months

Secondary Outcome Measures

Name	Time	Method
Frequency of epileptiform discharges	2 months	The frequency of the epileptiform discharges on EEGs evaluate at the baseline, after therapy, 1 and 2 months.
Amplitude of epileptiform discharges	2 monts	Amplitude of the epileptiform discharges on EEGs evaluate at the baseline, after therapy, 1 and 2 months.

Trial Locations

Locations (1)

Instituto Nacional de Neurología y Neurocirugía; 🇲🇽 Mexico City, DF, Mexico