What is the Registry?

The VNS Therapy™ Patient Outcome Registry was developed at the request of physicians who wanted immediate access to the most current, post-FDA approval data and experience of VNS Therapy. The Registry provides evidence of the long-term efficacy of VNS Therapy and is a voluntary patient outcome registry for patients implanted with VNS Therapy. The Registry is the first long-term patient outcome registry in epilepsy, and it includes quality-of-life and seizure control data. Registry data were collected at implantation and at 3, 6, 12, 18, and 24 months.

Physicians have access to long-term patient outcomes and can query the database for information based on particular patient characteristics, which can be helpful when considering a new patient for VNS Therapy. Clinicians are able to access their own Registry data, their center’s Registry data, and/or the entire Registry database via this website. To log on to the VNS Therapy Patient Outcome Registry database, please click here.