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Transcranial Direct Current Stimulation (tDCS) As A Tool For Prospective Responder Identification Before Vagus Nerve Stimulation (VNS) Implantation

Primary Purpose

Epilepsy

Status
Unknown status
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
transcranial direct current stimulation
Sponsored by
University of Luebeck
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Epilepsy focused on measuring Electroencephalography, Seizure frequency, Seizure severity

Eligibility Criteria

12 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age: 12 years and above
  • At least 2 years disease history
  • Refractory epilepsy:

    • Seizures are not completely responsive to longlasting antiepileptic treatment. At least 4 antiepileptic medicaments failed in mono or combined anticonvulsive regimen.
    • At least 4 seizures per week in the last month, despite adequate antiepileptic regimen.
    • Epilepsy surgery is not indicated or not accepted by the patient or by the parents of the patient.
  • A stable anticonvulsive regimen, defined as unchanged dose and type of the antiepileptic medication in the last month before tDCS and before VNS implantation.
  • Seizure diary is available and completed.
  • VNS implantation is planned within the next 2 months.

Exclusion Criteria:

  • Acute, symptomatic seizures (caused by tumor, stroke, acute encephalitis)
  • Uncontrolled medical problems (e.g. cardiovascular, nephrotic oder severe, chronic or severe acute disease)
  • Increased intracranial pressure for whatever reason
  • Implantation of metallic material (e.g. pacemaker, cochlear-implant)
  • Diseased or damaged skin over the scalp (e.g. Dermatitis)
  • Pregnancy
  • Known or supposed non-compliance
  • Age: less than 12 years

Sites / Locations

  • Pediatrics Department, University of LuebeckRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

Outcomes

Primary Outcome Measures

Correlation of tDCS effects in terms of EEG changes, number of seizures and seizure severity to VNS therapy outcome

Secondary Outcome Measures

To define criteria which will have predictive value for VNS therapy outcome.

Full Information

First Posted
February 11, 2008
Last Updated
January 27, 2010
Sponsor
University of Luebeck
Collaborators
Cyberonics, Inc., University Hospital, Bonn, University of Erlangen-Nürnberg Medical School, Epilepsycenter Bielefeld
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1. Study Identification

Unique Protocol Identification Number
NCT00625222
Brief Title
Transcranial Direct Current Stimulation (tDCS) As A Tool For Prospective Responder Identification Before Vagus Nerve Stimulation (VNS) Implantation
Study Type
Interventional

2. Study Status

Record Verification Date
January 2010
Overall Recruitment Status
Unknown status
Study Start Date
September 2007 (undefined)
Primary Completion Date
June 2010 (Anticipated)
Study Completion Date
June 2010 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
University of Luebeck
Collaborators
Cyberonics, Inc., University Hospital, Bonn, University of Erlangen-Nürnberg Medical School, Epilepsycenter Bielefeld

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the study is to establish tDCS as a prognostic tool to predict VNS therapy outcome among patients with pharmacoresistant epilepsy.
Detailed Description
In recent years it has been shown that many different brain stimulation techniques are effective in seizure reduction in epilepsy patients as well as in animal models of epilepsy. VNS is the method most often used with at least 45.000 patients implanted with this device worldwide. However, prediction of seizure outcome after VNS implantation is not possible in an individual patient so far. Recently, tDCS is increasingly used as a method to reduce seizure frequency in epileptic patients. Therefore it is hypothesized, that a positive effect after a single tDCS, in terms of short time seizure reduction and reduction of epileptic discharges in the EEG, could be predictive for epilepsy outcome after VNS implantation. In the proposed multicenter prognostic study we test the predictive value of tDCS for each patient with refractory epilepsy 1 week up to 2 months before VNS implantation. The effects of tDCS will be verified via a 15 minutes long routine EEG examination, performed immediately before and after tDCS, together with seizure diary and seizure severity scale, assessed 1 month before and 1 week after tDCS. A 6 months long observation period will follow the VNS implantation. At the end of the 6 months period seizure diary and seizure severity scale of the last month will be performed to measure VNS therapy outcome. On the basis of the described variables, immediate up to 1 week long tDCS effects will be correlated to 6 months long VNS therapy outcome.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epilepsy
Keywords
Electroencephalography, Seizure frequency, Seizure severity

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
transcranial direct current stimulation
Intervention Description
1mA, 15 Minutes, constant direct current
Primary Outcome Measure Information:
Title
Correlation of tDCS effects in terms of EEG changes, number of seizures and seizure severity to VNS therapy outcome
Time Frame
6 Months
Secondary Outcome Measure Information:
Title
To define criteria which will have predictive value for VNS therapy outcome.
Time Frame
6 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 12 years and above At least 2 years disease history Refractory epilepsy: Seizures are not completely responsive to longlasting antiepileptic treatment. At least 4 antiepileptic medicaments failed in mono or combined anticonvulsive regimen. At least 4 seizures per week in the last month, despite adequate antiepileptic regimen. Epilepsy surgery is not indicated or not accepted by the patient or by the parents of the patient. A stable anticonvulsive regimen, defined as unchanged dose and type of the antiepileptic medication in the last month before tDCS and before VNS implantation. Seizure diary is available and completed. VNS implantation is planned within the next 2 months. Exclusion Criteria: Acute, symptomatic seizures (caused by tumor, stroke, acute encephalitis) Uncontrolled medical problems (e.g. cardiovascular, nephrotic oder severe, chronic or severe acute disease) Increased intracranial pressure for whatever reason Implantation of metallic material (e.g. pacemaker, cochlear-implant) Diseased or damaged skin over the scalp (e.g. Dermatitis) Pregnancy Known or supposed non-compliance Age: less than 12 years
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jürgen Sperner, Prof. M.D.
Phone
+49-451-500-2605
Email
sperner@paedia.ukl.mu-luebeck.de
First Name & Middle Initial & Last Name or Official Title & Degree
Iren Orosz, M.D.
Phone
+49-451-500-4559
Email
orosz@paedia.ukl.mu-luebeck.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jürgen Sperner, Prof., M.D.
Organizational Affiliation
Pediatrics Department, University of Luebeck, Germany
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Iren Orosz, M.D.
Organizational Affiliation
Pediatrics Department, University of Luebeck, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Pediatrics Department, University of Luebeck
City
Luebeck
ZIP/Postal Code
23538
Country
Germany
Individual Site Status
Recruiting

12. IPD Sharing Statement

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Transcranial Direct Current Stimulation (tDCS) As A Tool For Prospective Responder Identification Before Vagus Nerve Stimulation (VNS) Implantation

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