Mainz Epilepsy Registry

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Brief Title

Mainz Epilepsy Registry

Official Title

Study on Disease Course and Quality of Life in Patients With Epilepsy (Mainz Epilepsy Registry)

Brief Summary

      Prospective longitudinal observational registry study of all patients with epilepsy treated
      in the Mainz Comprehensive Epilepsy and Sleep Medicine Center with the focus on the course of
      the disease and quality of life.

Detailed Description

      Clinical parameters of patients, such as onset of the disease, prior medication, disease
      severity, which are important for the data analysis also collected retrospectively before the
      initiation of the registry. Data on the quality of life is collected only prospectively.

Study Type

Observational [Patient Registry]

Primary Outcome

monthly seizure frequency after 6 months

Secondary Outcome

 Resilience Scale 13




no interventions, only observation


* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information

Recruitment Status


Estimated Enrollment


Start Date

February 1, 2018

Completion Date

January 31, 2024

Primary Completion Date

January 31, 2024

Eligibility Criteria

        Inclusion Criteria:

          -  Epileptic or psychogenic seizures

        Exclusion Criteria:

          -  age<18

          -  patients who cannot provide informed consent and don't have a legal guardian




18 Years - N/A

Accepts Healthy Volunteers



Yaroslav Winter, MD, MSc, +496131172234, [email protected]

Location Countries


Location Countries


Administrative Informations



Organization ID


Responsible Party

Principal Investigator

Study Sponsor

Johannes Gutenberg University Mainz

Study Sponsor

Yaroslav Winter, MD, MSc, Principal Investigator, Mainz Comprehensive Epilepsy and Sleep Medicine Center

Verification Date

February 2022