ZAGAL Study: Evaluating Effectiveness and Tolerability of Zonisamide as Adjunctive Therapy in Patients With Partial Onset Seizures Treated With Two Antiepileptic Drugs
NCT ID: NCT00659958
Last Updated: 2013-05-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
PHASE4
32 participants
INTERVENTIONAL
2008-04-30
2009-09-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
A Study to Evaluate the Safety and Efficacy of Zonisamide an Antiepileptic Drug as Monotherapy or Adjunctive Therapy in Treatment of Adult Patients With Partial, Generalized or Combined Seizures.
NCT01283256
Efficacy and Safety of Adjunctive Zonisamide in Myoclonic Seizures Associated With Idiopathic Generalised Epilepsy
NCT00693017
Efficacy and Safety of an add-on Treatment With Zonisamide in Adults With Focal Epileptic Seizures With or Without Secondary Generalization
NCT00165828
Open Label, Zonegran (Zonisamide) In Partial Onset Seizures
NCT00215592
A Study for Evaluating the Efficacy and Safety of Zonisamide and Lamotrigine (Lamictal) for Subjects With Refractory Simple Partial, Complex Partial or Partial With Secondary Generalized Seizures
NCT00292461
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
NON_RANDOMIZED
SINGLE_GROUP
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
Zonisamide
300 mg tablet. Maintenance dosing 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.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Zonisamide
300 mg tablet. Maintenance dosing 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.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Eisai FarmacĂȘutica S.A.
INDUSTRY
Eisai Inc.
INDUSTRY
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Jesus De Rosendo
Role: STUDY_CHAIR
EISAI Farmaceutica S.A. Head of Medical Department
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Complejo Hospitalario Universitario 'Juan Canalejo'
A Coruña, Galicia, Spain
C.H. A. Marcide Profesor Novoa Santos
Ferrol, Galicia, Spain
Centro Sanitario Complexo Hospitalario "XERAL-CALDE"
Lugo, Galicia, Spain
Hospital Comarcal de Monforte
Lugo, Galicia, Spain
Centro Sanitario Hospital Da Costa de Burela
Lugo, Galicia, Spain
Complejo Hospitalario de Ourense
Ourense, Galicia, Spain
Complejo Hospitalario de Pontevedra
Pontevedra, Galicia, Spain
Complejo Hospitalario Universitario Santiago de Compostela
Santiago de Compostela, Galicia, Spain
Complejo Hospitalario Universitario de Vigo (CHUVI), Hospital Meixoeiro
Vigo, Galicia, Spain
Hospital Povisa
Vigo, Galicia, Spain
Complejo Hospitalario Universitario de Vigo (CHUVI), Hospital Xeral-Cies
Vigo, Galicia, Spain
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
E2090-E044-407
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.