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External Trigeminal Nerve Stimulation for Epilepsy

Primary Purpose

Epilepsy, Seizure Disorders

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Trigeminal Nerve Stimulation
Sponsored by
Olive View-UCLA Education & Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Epilepsy focused on measuring partial seizures, poorly controlled epilepsy, intractable epilepsy, treatment resistant epilepsy, Trigeminal Nerve, Trigeminal Nerve Stimulation

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Ages 18 - 70;
  • No serious or progressive medical illness;
  • A history of intractable partial seizures;
  • At least two complex partial or tonic clonic generalized seizures per month in the last two consecutive months;
  • MRI or EEG consistent with localization-related or partial epilepsy;
  • Exposure to at least two antiepileptic drugs at adequate doses;
  • Concurrent use of at least one antiepileptic drug at adequate doses;
  • No change in antiepileptic dose for at least 30 days before study enrollment

Exclusion Criteria:

  • History of non-epileptic seizures;
  • Inability to maintain accurate seizure calendars (self or caregiver);
  • Frequent use of benzodiazepines for clusters defined as greater than four times a month;
  • History of facial pain or trigeminal neuralgia;
  • Concurrent vagus nerve stimulation;
  • Pregnancy

Sites / Locations

  • USC Department of Neurology
  • Olive View/UCLA Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Active

Control

Arm Description

Outcomes

Primary Outcome Measures

50% Responder Rate
Change in responder rate, at end of study (18 weeks) Absolute percent of subjects with 50% reduction in seizures, 18 weeks compared with 6 weeks Note, the number is not a mean or median, but a fixed percentage.
Time to the 4th Seizure
Number of Days to the 4th seizure
Change in Seizure Frequency
Percent change in seizure frequency from baseline

Secondary Outcome Measures

Response Ratio: Mean Percent Change in Seizures
Response Ratio: Mean Percent Change in seizures over the treatment period, where [T-B] / [T+B] x 100%, where T = seizure frequency during the treatment period, and B = seizure frequency during the baseline period.
Mood
Mean change in score on the Beck Depression Inventory. The Beck Inventory is a patient reported mood scale. The minimum score is 0, and the maximum score is 63. Scores of less than 10 are considered in the normal range. Scores above 10 are consistent with depression. Higher scores indicate higher degrees of depression, with scores of > 25 consistent with severe depression.

Full Information

First Posted
July 7, 2010
Last Updated
May 6, 2013
Sponsor
Olive View-UCLA Education & Research Institute
Collaborators
Epilepsy Foundation, Boston Scientific Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT01159431
Brief Title
External Trigeminal Nerve Stimulation for Epilepsy
Official Title
Randomized Double Blind Study of External Trigeminal Nerve Stimulation for Intractable Epilepsy
Study Type
Interventional

2. Study Status

Record Verification Date
May 2013
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
June 2011 (Actual)
Study Completion Date
June 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Olive View-UCLA Education & Research Institute
Collaborators
Epilepsy Foundation, Boston Scientific Corporation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study investigates a new therapy for epilepsy called Trigeminal Nerve Stimulation (TNS). TNS involves external electrical stimulation of sensory nerve located above the eyes and over the forehead. The purpose of this study is to determine if TNS is safe and effective using a rigorous randomized active-control clinical trial design in 50 people with epilepsy.
Detailed Description
Poorly controlled epilepsy is a disabling condition, affecting over one million Americans. Neurostimulation is a promising alternative for patients who have failed medical therapy, and who are not resective surgical candidates. Trigeminal Nerve Stimulation (TNS) is a novel form of neurostimulation, and has a strong antiepileptic effect in an animal model of seizures. Preliminary data in humans indicates TNS is well tolerated and may be effective in people with intractable epilepsy. TNS is an alternative mode of neurostimulation, because the Trigeminal Nerve can be stimulated in minimally-invasive fashion. This is a randomized double blind study of Trigeminal Nerve Stimulation, which compares high stimulation to an active control. Subjects with poorly controlled partial onset seizures who meet all inclusion and exclusion criteria, enter a 6-week baseline period, and then are randomized in double-blind fashion to high or low intensity stimulation for 18 weeks. 50 subjects are to be enrolled at two sites. Study outcomes are the following: Percent change in seizure frequency during the treatment period compared with the baseline (pre-treatment) period. Time to the 4th seizure The primary comparisons will be between and within groups.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Epilepsy, Seizure Disorders
Keywords
partial seizures, poorly controlled epilepsy, intractable epilepsy, treatment resistant epilepsy, Trigeminal Nerve, Trigeminal Nerve Stimulation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
50 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Active
Arm Type
Experimental
Arm Title
Control
Arm Type
Other
Intervention Type
Device
Intervention Name(s)
Trigeminal Nerve Stimulation
Intervention Description
External stimulation of the supraorbital branch of the Trigeminal Nerve using a digital TENs unit
Primary Outcome Measure Information:
Title
50% Responder Rate
Description
Change in responder rate, at end of study (18 weeks) Absolute percent of subjects with 50% reduction in seizures, 18 weeks compared with 6 weeks Note, the number is not a mean or median, but a fixed percentage.
Time Frame
Treatment period, 18 weeks (end of double blind period) compared with first 6 weeks
Title
Time to the 4th Seizure
Description
Number of Days to the 4th seizure
Time Frame
treatment period (18-weeks)
Title
Change in Seizure Frequency
Description
Percent change in seizure frequency from baseline
Time Frame
18 weeks
Secondary Outcome Measure Information:
Title
Response Ratio: Mean Percent Change in Seizures
Description
Response Ratio: Mean Percent Change in seizures over the treatment period, where [T-B] / [T+B] x 100%, where T = seizure frequency during the treatment period, and B = seizure frequency during the baseline period.
Time Frame
18 weeks
Title
Mood
Description
Mean change in score on the Beck Depression Inventory. The Beck Inventory is a patient reported mood scale. The minimum score is 0, and the maximum score is 63. Scores of less than 10 are considered in the normal range. Scores above 10 are consistent with depression. Higher scores indicate higher degrees of depression, with scores of > 25 consistent with severe depression.
Time Frame
18-weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Ages 18 - 70; No serious or progressive medical illness; A history of intractable partial seizures; At least two complex partial or tonic clonic generalized seizures per month in the last two consecutive months; MRI or EEG consistent with localization-related or partial epilepsy; Exposure to at least two antiepileptic drugs at adequate doses; Concurrent use of at least one antiepileptic drug at adequate doses; No change in antiepileptic dose for at least 30 days before study enrollment Exclusion Criteria: History of non-epileptic seizures; Inability to maintain accurate seizure calendars (self or caregiver); Frequent use of benzodiazepines for clusters defined as greater than four times a month; History of facial pain or trigeminal neuralgia; Concurrent vagus nerve stimulation; Pregnancy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christopher M DeGiorgio, MD
Organizational Affiliation
UCLA Department of Neurology
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Christi Heck, MD
Organizational Affiliation
University of Southern California
Official's Role
Principal Investigator
Facility Information:
Facility Name
USC Department of Neurology
City
Los Angeles
State/Province
California
ZIP/Postal Code
90033
Country
United States
Facility Name
Olive View/UCLA Medical Center
City
Sylmar
State/Province
California
ZIP/Postal Code
91342
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
19273830
Citation
DeGiorgio CM, Murray D, Markovic D, Whitehurst T. Trigeminal nerve stimulation for epilepsy: long-term feasibility and efficacy. Neurology. 2009 Mar 10;72(10):936-8. doi: 10.1212/01.wnl.0000344181.97126.b4. No abstract available.
Results Reference
background
PubMed Identifier
23365066
Citation
DeGiorgio CM, Soss J, Cook IA, Markovic D, Gornbein J, Murray D, Oviedo S, Gordon S, Corralle-Leyva G, Kealey CP, Heck CN. Randomized controlled trial of trigeminal nerve stimulation for drug-resistant epilepsy. Neurology. 2013 Feb 26;80(9):786-91. doi: 10.1212/WNL.0b013e318285c11a. Epub 2013 Jan 30.
Results Reference
result

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External Trigeminal Nerve Stimulation for Epilepsy

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