Epilepsy Clinical Trial
Official title:
Post-authorization, Observational and Prospective Follow up Study to Evaluate Effectiveness and Tolerability of Zonisamide as Adjunctive Therapy in Patients With Partial Onset Seizures Treated With Two Antiepileptic Drugs
The purpose of this study is to acquire additional information about the appropriate level of dosing of Zonisamide when it is prescribed for patients with partial onset epileptic crisis who are already being treated with two other antiepileptic drugs.
Patients from both sexes, 18 to 65 years of age, diagnosed with simple or complex partial
onset epileptic crisis defined according to the International League Against Epilepsy (ILAE)
criteria, with a minimum of two seizures within the 4 previous weeks, a stable treatment
with two antiepileptic drugs for at least 12 weeks, and capable and willing to give their
informed consent, will be included in the study.
To these patients, physicians will prescribe zonisamide in the following manner: Titration
period of 12 weeks, at the end of which all patients must be taking 300 mg. Maintenance
doses period of 12 weeks, at the beginning of which, physicians will decide to keep the 300
mg dose from the titration period, lower it to 200 mg, or take it up to 400 mg. Six weeks
later within this period, a decision will be made to raise the 400 mg doses up to 500 mg if
considered necessary and tolerable.
Drugs will be prescribed by the physician and purchased by the patient.
;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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