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Psychiatric assessment prior to and after switch from levetiracetam to brivaracetam: a questionnaire study

Psychiatric assessment prior to and after switch from levetiracetam to brivaracetam: a questionnaire study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00022128
Enrollment
50
Registered
2020-06-05
Start date
2020-06-07
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

G40.2 G40.3

Interventions

Group 1: The assessment of psychiatric problems in patients with epilepsy who switch from levetiracetam to brivaracetam with the examination of the following parameters: SCL-90-S, BDI II, AEP and Qoli

Sponsors

Epilepsiezentrum Kork
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Participants with minimum age of 18 years and a diagnosis of epilepsy according to the 1989 International League Against Epilepsy (ILAE) classification 2. Participants receiving levetiracetam with an unchanged dose within 4 weeks. 3. The decision to switch from levetiracetam to brivaracetam will be made by the physician before and irrespective of his/her decision to include the participant in the study

Exclusion criteria

Exclusion criteria: 1. Participants with known psychogenic non-epileptic seizures 2. Participants had already received brivaracetam in the past 3. Participants with a medical or a psychiatric condition that, in the opinion of the Investigator, could jeopardize or compromise the patient’s own ability to participate in the study: for example patients with status epilepticus, acute psychosis, acute respiratory distress, or participants with significant cognitive disorders etc.

Design outcomes

Primary

MeasureTime frame
The aim of this study is to investigate a psychiatric change in epilepsy patients switching from levetiracetam to brivaracetam using the following parameters (Questionnaires): SCL-90-S, BDI II, AEP and Qolie31-P, between June 2020 and June 2021. Participants in the study will fill the questionnaires prior to and 8 days after switching to brivaracetam.

Countries

Germany

Contacts

Public ContactTassanai Intravooth

Epilepsiezentrum Kork

tintravooth@epilepsiezentrum.de00497851842272

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026