Skip to content

Genetic and pharmacogenetic analyses of patients with epilepsy and related diseases

Genetic and pharmacogenetic analyses of patients with epilepsy and related diseases

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00025480
Enrollment
1200
Registered
2021-09-17
Start date
2021-08-01
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 F45.0

Interventions

Group 1: Clinical data and DNA samples will be collected continuously throughout the study period.

Sponsors

Universitätsklinikum der RWTH Aachen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0 Years to 105 Years

Inclusion criteria

Inclusion criteria: - Individuals with diagnosis of epilepsy syndrome or related paroxysmal disorder - 1st and 2nd degree relatives of individuals with diagnosis of epilepsy syndrome or related paroxysmal disorder

Exclusion criteria

Exclusion criteria: Individuals who are not able to give informed consent by themselves or by a legal guardian

Design outcomes

Primary

MeasureTime frame
Genetic analysis of collected samples.

Secondary

MeasureTime frame
Identification of genetic variants for further functional studies.

Countries

Germany

Contacts

Public ContactStefan Wolking

Universitätsklinikum der RWTH Aachen

swolking@ukaachen.de0241-80-85829

Outcome results

None listed

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