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Clinical Trials/ISRCTN72921325
ISRCTN72921325Completed未知

A post-market, long-term, prospective, observational, multi-site outcome study to assess the clinical course and seizure reduction of patients treated with adjunctive vagus nerve stimulation therapy in France

ivaNova Belgium N.V.0 sites150 target enrollmentStarted: April 26, 2013Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
150

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational

Eligibility Criteria

Sex
All

Inclusion Criteria

  • 1. All newly patients implanted with a VNS device
  • 2. Patients must have received the information letter and agreed that their data will be collected and transmitted to Cyberonics for analysis

Exclusion Criteria

  • Does not meet inclusion criteria
  • The investigator should refer to the instructions for VNS Therapy use

Investigators

Sponsor
ivaNova Belgium N.V.

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