Vagus Nerve Stimulation Clinical Outcomes Measured Prospectively in Patients Stimulated
- Conditions
- Epilepsy
- Registration Number
- NCT01281293
- Lead Sponsor
- Cyberonics, Inc.
- Brief Summary
Vagus Nerve Stimulation (VNS) Therapy has been approved marked for the treatment of epilepsy since 1994. This post-market study is designed to follow the clinical course and outcomes for patients with refractory seizures treated with adjunctive VNS Therapy. Seizure frequency, seizure severity, side effects burden, depressive symptoms, global impressions, and health care utilization will be evaluated. The results of this study will provide data to guide physicians and their patients in the use of VNS Therapy for patients with refractory seizures who have failed initial trials of anti-epileptic drug (AED) therapy. The data being collected is not for the purposes of confirmatory assessment.
- Detailed Description
Minimum ages eligible for the E-103 study is at least 7 years outside of the US, consistent with "Non-US" labeling and 12 years for sites in the US.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 124
Patients enrolled in the study must meet all of the following criteria at Visit 1:
(Baseline) if Screening Incl/Excl is omitted:
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Patients must agree to be treated with VNS Therapy. The decision to treat with VNS Therapy must have been made independent of and prior to participation in the study.
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Patients participating at Sites not located in the US must follow the "Non-US" labeling and be at least 7 years or older and whose epileptic disorder is dominated by partial seizures (with or without secondary generalization) or generalized seizures that are refractory to antiepileptic medications; patients participating at Sites located in the United States must be 12 years or older and have partial onset seizures or must follow the indication for use statement (for VNS Therapy) in the country of origin.
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Patient and/or caregiver must be able to give accurate seizure counts, health outcomes information, and complete study instruments with minimal assistance.
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Patient or legal guardian understands study procedures and voluntarily signs an informed consent and in the United States a Health Insurance Portability and Accountability Act (HIPAA) authorization in accordance with institutional policies. In the event that the patient is under the age of 18 the patient will also be required to sign an assent affirming their agreement to participate in research according to local IRB requirements. Similar authorization is required per EC requirements, or equivalent authority.
Additional Continuation Criteria to be evaluated at Visit 2 (Baseline):
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Patient must be taking at least 1 anti-epileptic drug treatment and stable on said medications for at least 8 weeks (56 days) prior to baseline. (Rescue medication may be allowed on a case-by case basis with Cyberonics approval.)
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Patient must have a minimum frequency of 3 seizures (excluding absence seizures, simple partial seizures and myoclonic jerks) per month (average over 2 months) prior to baseline; maximum frequency is 20 seizures per day.
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Patient must have no more than 4 weeks between seizures (over 2 months) prior to baseline.
Patients with any of the following will not be eligible for enrollment:
- Patient currently uses, or is expected to use during the study, short-wave diathermy, microwave diathermy, or therapeutic ultrasound diathermy.
- Patient is expected to require full body magnetic resonance imaging during the clinical study.
- Patient has a progressive neurological condition (e.g. brain tumor etc.).
- In the investigator's opinion, the inability of the patient, legal guardian or reluctance of the child to comply with the frequency of clinic visits during the treatment phase.
- In the investigator's opinion, the patient has a history of noncompliance for seizure diary completion.
- Patient is currently using an investigational device or pharmacologic medication not approved by either EU or US regulatory authority.
- Patient has had a previous VNS Therapy implant.
- In the investigator's opinion, the patient is suicidal.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Two-Year Clinical Follow-up 27 months To follow the clinical course of patients with refractory seizures treated with adjunctive VNS Therapy over a two-year follow-up period.
- Secondary Outcome Measures
Name Time Method Efficacy and Safety 27 months 1. To evaluate over time the efficacy of best medical practice with adjunctive VNS Therapy in patients with refractory seizures.
2. To evaluate over time the safety and tolerability of best medical practice with adjunctive VNS Therapy in patients with refractory seizures.
Trial Locations
- Locations (20)
Emory Healthcare
🇺🇸Atlanta, Georgia, United States
University of Illinois College of Medicine at Peoria
🇺🇸Peoria, Illinois, United States
University of Louisville Hospital
🇺🇸Louisville, Kentucky, United States
Epilepsieklinik Tabor - Ladeburger Straße 15
🇩🇪Berlin, Germany
Covenant Hospital
🇺🇸Lubbock, Texas, United States
UZ Gasthuisberg
🇧🇪Leuven, Belgium
St. Luke's Milwaukee
🇺🇸Milwaukee, Wisconsin, United States
Universitätsklinikum Schleswig-Holstein Campus Kiel
🇩🇪Kiel, Germany
Albert-Ludwigs-Universität Freiburg
🇩🇪Freiburg, Germany
Birmingham Children's Hospital
🇬🇧Birmingham, United Kingdom
John Radcliffe Hospital
🇬🇧Oxford, United Kingdom
Southmead Hospital Bristol
🇬🇧Bristol, United Kingdom
Foundation Trust Queen Elizabeth Hospital Birmingham
🇬🇧Birmingham, United Kingdom
National Hospital for Neurology & Neurosurgery - UCLH
🇬🇧London, United Kingdom
Salford Royal Hospital
🇬🇧Salford, United Kingdom
Royal Hallamshire Hospital
🇬🇧Sheffield, United Kingdom
Great Ormond Street Hospital for Children NHS Foundation Trust
🇬🇧London, United Kingdom
Cornell University
🇺🇸New York, New York, United States
Sheba Medical Center
🇮🇱Ramat Gan, Israel
Vanderbilt University Medical Center
🇺🇸Nashville, Tennessee, United States