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Safety and Efficacy of Topamax Versus Carbamazepine in Benign Rolandic Epilepsy

Primary Purpose

Epilepsy, Rolandic

Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
topamax
Sponsored by
Janssen Korea, Ltd., Korea
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Epilepsy, Rolandic focused on measuring Benign rolandic epilepsy, Topiramate

Eligibility Criteria

5 Years - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Subjects whose guardians submitted written consent Subjects with more than 2 seizures in last 1 year Subjects showing one of the following additional criteria Psychological burden due to seizure Seizure in daytime More than 3 seizures in last 6 month Convulsive seizure Exclusion Criteria: Abnormalities on MRI, EEG Mental retardation History of seizure relapse Seizures due to organic causes Medically serious acute or chronic disease or progressive and degenerative disorders Patients who have received an investigational medication

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Seizure-free rate at 24 weeks in comparison of topiramate to carbamazepine

    Secondary Outcome Measures

    In comparison of topiramate to carbamazepine, Intellectual Functioning : KEDI-WISC (Korean Educational Development Institute Wechsler Intelligence Scale for Children-Revised)

    Full Information

    First Posted
    September 13, 2005
    Last Updated
    January 31, 2011
    Sponsor
    Janssen Korea, Ltd., Korea
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00216567
    Brief Title
    Safety and Efficacy of Topamax Versus Carbamazepine in Benign Rolandic Epilepsy
    Official Title
    A Randomized, Open Label, Comparative, Multi-center Clinical Trial to Determine the Efficacy and Safety of Topiramate Comparing With Carbamazepine in Benign Rolandic Epilepsy.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2011
    Overall Recruitment Status
    Completed
    Study Start Date
    December 2002 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    February 2006 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Janssen Korea, Ltd., Korea

    4. Oversight

    5. Study Description

    Brief Summary
    The purpose of this study is to determine the efficacy and safety of Topiramate in comparison to Carbamazepine in Benign rolandic epilepsy.
    Detailed Description
    Benign rolandic epilepsy (BRE) is a common seizure disorder confined solely to children. The disorder is marked clinically by nocturnal generalized tonic-clonic seizures and diurnal seizures consisting of simple partial seizures consisting of brief unilateral facial clonic activity, dysphasia, and drooling. The EEG abnormalities are unique, consisting of generally high amplitude, centrotemporal spikes that are activated by sleep. The seizures typically begin in the first decade and almost always stop by age 16 years. The seizures are usually infrequent although clusters of seizures do occur. When the physician elects to treat, the seizures are usually easily controlled. This is a randomized, open label, active controlled, multi-center based clinical trial to determine the efficacy and safety of Topiramate comparing with Carbamazepine in Benign rolandic epilepsy. The study hypothesis is that topiramate will be more effective in treatment of Benign rolandic epilepsy than Carbamazepine, as evaluated by seizure-free rate at 24 weeks and Intellectual Functioning : KEDI-WISC (Korean Educational Development Institute Wechsler Intelligence Scale for Children-Revised) and is generally well-tolerated. Topiramate (target dose) 4mg/kg/day, B.I.D, oral, for 24 weeks, carbamazepine(target dose) 30mg/kg/day, B.I.D, oral, for 24 weeks.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Epilepsy, Rolandic
    Keywords
    Benign rolandic epilepsy, Topiramate

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 4
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    114 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    topamax
    Primary Outcome Measure Information:
    Title
    Seizure-free rate at 24 weeks in comparison of topiramate to carbamazepine
    Secondary Outcome Measure Information:
    Title
    In comparison of topiramate to carbamazepine, Intellectual Functioning : KEDI-WISC (Korean Educational Development Institute Wechsler Intelligence Scale for Children-Revised)

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    5 Years
    Maximum Age & Unit of Time
    15 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Subjects whose guardians submitted written consent Subjects with more than 2 seizures in last 1 year Subjects showing one of the following additional criteria Psychological burden due to seizure Seizure in daytime More than 3 seizures in last 6 month Convulsive seizure Exclusion Criteria: Abnormalities on MRI, EEG Mental retardation History of seizure relapse Seizures due to organic causes Medically serious acute or chronic disease or progressive and degenerative disorders Patients who have received an investigational medication
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Janssen Korea, Ltd. Clinical Trial
    Organizational Affiliation
    Janssen Korea, Ltd.
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Learn more about this trial

    Safety and Efficacy of Topamax Versus Carbamazepine in Benign Rolandic Epilepsy

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