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Belgian Drug-utilization Study to Evaluate the Use of VIMPAT® as Adjunctive Treatment of Partial Onset Seizures in Subjects Aged 16 and Older

Seizures Clinical Trial

Official title:
Multi-center, Observational, Drug-utilization Study in Belgium to Evaluate the Use of VIMPAT® in Clinical Practice as Adjunctive Treatment of Partial Onset Epilepsy in Subjects Aged 16 and Older.

Clinical Trial Summary

Observational study at the request of the Belgian Institut National d'Assurance Maladie-Invalidité / Rijksinstituut voor Ziekte-en Invaliditeits Verzekering INAMI/RIZIV:

- type of patient treated with VIMPAT®

- VIMPAT® dose

- Effect of VIMPAT® on evolution of seizure control

- Persistence rate at 6 months in terms of treatment duration

- Discontinuation rate

- Description of any changes in other epilepsy therapies

- Safety and tolerability

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01236001
Study type Observational
Source UCB Pharma
Contact
Status Completed
Phase N/A
Start date September 2010
Completion date March 2012
View Details
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