Patient Preference in Epilepsy Monotherapy: A Non-interventional Study

  • Research type

    Research Study

  • Full title

    Patient Preference in Epilepsy Monotherapy - A Non-interventional Study of Vimpat® (Lacosamide) and other AEDs in the treatment of Partial onset seizures Including a Discrete Choice Experiment Surrounding Actual Treatment Decisions and Experiences

  • IRAS ID

    226181

  • Contact name

    John Paul Leach

  • Contact email

    JohnPaul.Leach@ggc.scot.nhs.uk

  • Sponsor organisation

    UCB BIOSCIENCES GmbH

  • Duration of Study in the UK

    2 years, 0 months, 1 days

  • Research summary

    There is limited real world data available on lacosamide (LCM; Vimpat® ) monotherapy in medical practice for the treatment of partial onset seizures. LCM monotherapy refers to treating patients with a single drug (i.e. only LCM and no other combination drug). As one of the primary aims, this is the first prospective real world study collecting data on patients treated with LCM monotherapy, designed to expand the knowledge base after launch of LCM as monotherapy in the European Union (EU). This study will collect information on Anti-epileptic drug (AED) effectiveness, cognitive functioning (using EpiTrack® ),quality of life, and patient comorbidities, as well as safety, in patients on LCM monotherapy. The study will also collect data on other AED monotherapy. Analysis of the data from this study will provide real world insight into individual AED monotherapy treatment of partial-onset seizures in relation to important patient characteristics.

  • REC name

    North West - Liverpool Central Research Ethics Committee

  • REC reference

    17/NW/0284

  • Date of REC Opinion

    5 May 2017

  • REC opinion

    Favourable Opinion