Neurostimulation to the Vagus Nerve for the Reduction in Frequency of Seizures Associated With Epilepsy

NCT ID: NCT01910129

Last Updated: 2019-04-23

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 13 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2013-07-31
• Study Completion Date: 2014-10-31

Brief Summary

The purpose of this study is to see the effects of non-invasive vagal nerve stimulation for the reduction in frequency of seizure associated with epilepsy in subjects 18 or older.

Detailed Description

The purpose of the study is to determine the effects of non-invasive vagus nerve stimulation for the reduction in frequency of seizure associated with epilepsy in subjects 18 or older. Subjects will record 4 weeks of baseline seizure activity before being randomized for a period of 8 weeks to receive and active treatment to an active-sham treatment. All subjects will then receive another 8 weeks of active treatment.

Conditions

Seizure

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: PREVENTION
• Blinding Strategy: DOUBLE

Study Groups

gammaCore

Active stimulation treatment

Group Type: ACTIVE_COMPARATOR

gammaCore

Intervention Type: DEVICE

vagal verve stimulation 3 times a day 8 hours apart

sham gammaCore

Inactive stimulation treatment

Group Type: PLACEBO_COMPARATOR

gammaCore

Intervention Type: DEVICE

vagal verve stimulation 3 times a day 8 hours apart

Interventions

gammaCore

vagal verve stimulation 3 times a day 8 hours apart

Intervention Type: DEVICE

Eligibility Criteria

Inclusion Criteria

1. The patient is diagnosed with epilepsy with; primary generalized tonic-clonic or partial complex or simple complex or focal onset seizures, with or without secondary generalization.

2. The patient's present antiepileptic drug (AED) therapy is ineffective or intolerable

3. The patient is receiving a stable dose of up to 2 oral AED medication(s) and is not expected to have any change in his/her baseline AED treatment during the treatment period.

4. The patient is having more than 2 recordable seizures a month.

Exclusion Criteria

1. The patient has had status epilepticus within the last six months.

2. The patient has had epilepsy surgery or a VNS implant.

3. The patient has had a history or presence of seizures occurring only in clusters (too frequently or indistinctly separated to be reliably counted).

4. The patient has had 4 weeks continuous seizure freedom last 2 months.

5. The patient has psychogenic non-epileptic seizures (PNES) seizures.

6. The patient has a concomitant progressive CNS disease including progressive myoclonus epilepsy.

7. The patient has a significant history of cardiac, renal, neurologic (other than epilepsy), psychiatric, oncologic, endocrinologic, metabolic, or hepatic disease, which would adversely affect their participation in this study.

8. The patient has had an episode of status epilepticus within 4 weeks of Screening.

10. Has a lesion (including lymphadenopathy), dysaesthesia, previous surgery or abnormal anatomy at the GammaCore treatment site.

11. Has known or suspected severe atherosclerotic cardiovascular disease, severe carotid artery disease (e.g. bruits or history of TIA or CVA), congestive heart failure (CHF), known severe coronary artery disease or recent myocardial infarction.

12. Has an abnormal baseline ECG (e.g. second and third degree heart block, atrial fibrillation, atrial flutter, recent history of ventricular tachycardia or ventricular fibrillation, or clinically significant premature ventricular contraction).

13. Has had a previous bilateral, right, or left cervical vagotomy. 14. Has uncontrolled high blood pressure. 15. Is currently implanted with an electrical and/or neurostimulator device, including but not limited to cardiac pacemaker or defibrillator, vagal neurostimulator, deep brain stimulator, spinal stimulator, bone growth stimulator, or cochlear implant.

16. Has a history of carotid endarterectomy or vascular neck surgery on the right side.

17. Has been implanted with metal cervical spine hardware or has a metallic implant near the GammaCore stimulation site.

18. Has a recent or repeated history of syncope. 19. Has a known history or suspicion of substance abuse or addiction. 20. In the opinion of the investigator/research staff the subject is incapable of operating the GammaCore device as intended and performing the data collection procedures.

21. Is pregnant, nursing, thinking of becoming pregnant in the next 9 months, or of childbearing years and is unwilling to use an accepted form of birth control.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 70 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

ElectroCore INC

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Roy Beran, Professor

Role: PRINCIPAL_INVESTIGATOR

Locations

Southern Neurology

Kogarah, New South Wales, Australia

Strategic Health Evaluators

Sydney, New South Wales, Australia

Countries

Australia

Other Identifiers

173/2013

Identifier Type: OTHER

Identifier Source: secondary_id

E-AU-01

Identifier Type: -

Identifier Source: org_study_id