Clinical Trial: European Registry of Anti-Epileptic Drug Use in Patients With Lennox-Gastaut Syndrome (LGS)
Study Status: Completed
Recruit Status: Completed
Study Type: Observational
Official Title: European Registry of Anti-epileptic Drug Use in Patients With Lennox-Gastaut Syndrome (LGS).
Brief Summary: This is a registry study, where sites will enter patients with LGS who require a modification in anti-epileptic therapy (either the addition of another anti-epileptic drug, or the change of one drug to another). This will include patients who are started on rufinamide. Patients will be reviewed according to local practice, but it is envisaged that review will occur at approximately one month, three months and six months, and then every six months. Upon entry to the registry baseline details concerning disease severity, diagnosis, prior therapy, and developmental assessment will be recorded. On each subsequent visit the patient (usually through their caregiver) will be asked about current medication, general seizure profile, any seizures deemed to be of medical significance, tolerability, AEs (including suicidal-related events), and healthcare resource utilisation.
Detailed Summary:
Sponsor: Eisai Limited
Current Primary Outcome: Safety during the use of rufinamide and other anti-epileptic drugs [ Time Frame: At least three years ]
Original Primary Outcome: Same as current
Current Secondary Outcome: Long term use of rufinamide, and other anti-epileptic drugs [ Time Frame: At least three years ]
Original Secondary Outcome: Long term use of rufinamide, and other anti-epileptic drugs [ Time Frame: At least three years ]
Information By: Eisai Inc.
Dates:
Date Received: November 18, 2013
Date Started: June 2008
Date Completion:
Last Updated: May 3, 2016
Last Verified: May 2016