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
About this trial
This is an interventional treatment trial for Epilepsy, Rolandic focused on measuring Benign rolandic epilepsy, Topiramate
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
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
NCT ID
NCT00216567
First Posted
September 13, 2005
Last Updated
January 31, 2011
Sponsor
Janssen Korea, Ltd., Korea
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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