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The Genetics of epilepsy

The Genetics of epilepsy - Genetics of epilepsy

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON35608
Enrollment
500
Registered
2010-06-25
Start date
2010-07-22
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Epilepsy

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
12 Years to 99 Years

Inclusion criteria

Inclusion criteria: - Any patient regardless of age or gender willing and able to provide informed consent ;- Children and persons unable to consent may be included if their parents or legal representative provide informed assent ;- A firm diagnosis of epilepsy based either on history, clinical examination or EEG regardless of type with a history of at least two independent epileptic seizures. ;- Etiological diagnosis supported by imaging, whenever appropriate

Exclusion criteria

Exclusion criteria: - Patient unwilling to provide consent or if parents or legal representative are unwilling to assent. ;- Diagnosis of epilepsy not corroborated by ancillary investigations ;- Age under 12 years

Design outcomes

Primary

MeasureTime frame
Genetic variation in genes that potentially predispose to epilepsy, yet have limited predictive value at an invidual level.

Secondary

MeasureTime frame
None

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)