A Study of the Efficacy and Safety of Topiramate as "Add on" Treatment in Epilepsy Patients With Primary Generalized Tonic-clonic Seizures
Topiramate Clinical Trial in Primary Generalized Tonic-Clonic Seizures
1 other identifier
interventional
80
0 countries
N/A
Brief Summary
The purpose of this study is to evaluate the effectiveness and safety of topiramate as an add-on therapy in epilepsy patients with uncontrolled primary generalized tonic-clonic seizures, who are taking 1 or 2 standard antiepileptic drugs.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_3
Started Mar 1994
Longer than P75 for phase_3
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 1994
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 1999
CompletedFirst Submitted
Initial submission to the registry
October 7, 2005
CompletedFirst Posted
Study publicly available on registry
October 12, 2005
CompletedJune 8, 2011
January 1, 2011
October 7, 2005
June 6, 2011
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Percent reduction from baseline in primary generalized tonic-clonic (PGTC) seizure rates in the double-blind phase.
Secondary Outcomes (1)
Percent of treatment responders; safety evaluations conducted throughout the study.
Interventions
Eligibility Criteria
You may qualify if:
- Body weight \>25 kilograms (55 pounds)
- diagnosis of primary generalized epilepsy
- must have primary generalized tonic-clonic (PGTC) seizures treated with 1 or 2 antiepileptic drugs
- must have three primary generalized tonic-clonic (PGTC) seizures during baseline period, with at least 1 during each 28-day period of baseline
- females must not have had their first menstrual period or be postmenopausal, or are physically incapable of child bearing, or if of child bearing potential, sexually abstinent, or using adequate birth control measures, and have a negative pregnancy test before study entry.
You may not qualify if:
- Patients who do not have epilepsy, such as those with a treatable cause of seizure (for example active infection or cancer)
- patients with progressive disorders (for example, active infection, cancer or metabolic disturbance)
- patients diagnosed with Lennox-Gastaut syndrome
- history of seizures occurring in only cluster patterns (numerous seizures occurring over a short period of time \[\<30 minutes\])
- documented history (previous 3 months) of generalized tonic-clonic status epilepticus (status epilepticus is a prolonged seizure or seizures repeated frequently over 20 to 30 minutes so that recovery between episodes does not occur) while receiving appropriate antiepileptic medication
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (1)
Biton V, Montouris GD, Ritter F, Riviello JJ, Reife R, Lim P, Pledger G. A randomized, placebo-controlled study of topiramate in primary generalized tonic-clonic seizures. Topiramate YTC Study Group. Neurology. 1999 Apr 22;52(7):1330-7. doi: 10.1212/wnl.52.7.1330.
PMID: 10227614RESULT
Related Links
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Johnson & Johnson Pharmaceutical Research & Development, L.L. C. Clinical Trial
Johnson & Johnson Pharmaceutical Research & Development, L.L.C.
Study Design
- Study Type
- interventional
- Phase
- phase 3
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- INDUSTRY
Study Record Dates
First Submitted
October 7, 2005
First Posted
October 12, 2005
Study Start
March 1, 1994
Study Completion
December 1, 1999
Last Updated
June 8, 2011
Record last verified: 2011-01