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Pharmacogenetics and epilepsy; analyse van de respons op lamotrigine

Pharmacogenetics and epilepsy; analyse van de respons op lamotrigine - Pharmacogenetics of lamotrigine as an antiepileptic drug

Status
Unknown
Phases
Phase 4
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON29964
Enrollment
200
Registered
2006-10-30
Start date
Unknown
Completion date
Unknown
Last updated
2024-06-18

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

Stichting Epilepsie Instellingen Nederland (SEIN)
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: General inclusion criteria 1. Adult patients with cryptogenic or symptomatic localization-related epilepsy, manifesting in generalized tonic-clonic, complex partial and/or simple partial seizures. 2. Patients that are able to understand the written information about the study and are able to give informed consent.

Exclusion criteria

Exclusion criteria: Exclusion criteria: 1. Patients failing valproate due to other reasons than persisting seizures despite a maximum tolerated dose (i.e. failure due to adverse effects on a starting dose of valproate, failure due to non-compliance etc). 2. Patients with generalized epilepsy and/or generalized absence-seizures and /or myoclonic seizures. 3. Acute or progressive neurological disease. 4. History of psychiatric disease or substance addiction.

Design outcomes

Primary

MeasureTime frame
Presence of selected polymorphisms in the three patient groups.

Secondary

MeasureTime frame
Number of antiepileptic drugs used; epilepsy subtype; seizure type.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)