VNS Therapy Automatic Magnet Mode Outcomes Study in Epilepsy Patients Exhibiting Ictal Tachycardia (E-37)
Status: | Completed |
---|---|
Conditions: | Cardiology, Neurology, Epilepsy |
Therapuetic Areas: | Cardiology / Vascular Diseases, Neurology, Other |
Healthy: | No |
Age Range: | 12 - Any |
Updated: | 4/21/2016 |
Start Date: | July 2013 |
End Date: | August 2015 |
VNS Therapy Automatic Magnet Mode Outcomes Study in Epilepsy Patients Exhibiting Ictal Tachycardia
Obtain baseline clinical outcome data (Stage 1) upon which to base a subsequent study (Stage
2) of the Model 106 VNS implantable pulse generator
2) of the Model 106 VNS implantable pulse generator
Prospective, observational, un-blinded, multi-site study designed to collect data on
patients implanted with a Model 106 VNS Therapy System from baseline through an EMU stay of
up to 5 days, and 6-month follow-up. After the 6-month follow-up, patients will continue
follow-up for safety for approximately two years or until final regulatory approval of the
product.
patients implanted with a Model 106 VNS Therapy System from baseline through an EMU stay of
up to 5 days, and 6-month follow-up. After the 6-month follow-up, patients will continue
follow-up for safety for approximately two years or until final regulatory approval of the
product.
Inclusion Criteria:
- Patients with a clinical diagnosis of medically refractory epilepsy with partial
onset seizures suitable for implantation with the VNS Therapy System.
- Patients willing to undergo an EMU evaluation for a period of at least three days
with activation of the AMM feature during that time.
- Patients must be at least 12 years old.
- Patients must be in good general health and ambulatory.
- Patient or guardian must be willing and able to complete informed consent/assent.
Exclusion Criteria:
- Patients have had a bilateral or left cervical vagotomy.
- Patients currently using, or are expected to use, short-wave diathermy, microwave
diathermy, or therapeutic ultrasound diathermy.
- A VNS Therapy System implant would (in the investigator's judgment) pose an
unacceptable surgical or medical risk for the patient.
- Patients expected to require full body magnetic resonance imaging (MRI).
- Patients have a history of implantation of the VNS Therapy.
- Patients with an IQ known or estimated to be < 70, history of depression requiring
hospitalization, or suicidality as defined by DSM IV-TR that in the investigator's
judgment would pose an unacceptable risk for the patient or prevent the patient's
successful completion of the study.
- Patients with a history of status epilepticus within 1 year of study enrollment.
- Patients with known clinically meaningful cardiovascular arrhythmias as well as
patients with clinically meaningful cardiovascular arrhythmias determined by a
24-hour Holter recording obtained during the baseline period.
- Patients dependent on alcohol or narcotic drugs as defined by DSM IV-TR within the
past 2 years.
- Patients with a history of psychogenic non-epileptic seizures.
- Women who are pregnant. Women of childbearing age must take a pregnancy test and
agree to use an approved method of contraception during the study.
- Patients currently enrolled in another investigational study.
We found this trial at
15
sites
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials
Click here to add this to my saved trials