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| Name | Class |
|---|---|
| Janssen Korea, Ltd., Korea | INDUSTRY |
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The Objective of this study is to compare 2-year retention rate of topiramate, levetiracetam and oxcarbazepine in a long term epilepsy treatment.
Primary objective The Objective of this study is to compare 2-year retention rate of topiramate, levetiracetam and oxcarbazepine in a long term epilepsy treatment.
Secondary objective The main secondary objective of this study is to evaluate confounding factors associated with retention rate of topiramate compared with other anticonvulsants.
Baseline characteristics
Treatment regimen
Other secondary objectives
The other secondary objectives of this study are to compare followings by each medication:
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Topiramate | Subjects who newly visited to the investigator institution during January 1st 2006 to December 31st of 2010 and began their treatment with topiramate as mono or add-on therapy with conventional drugs. | ||
| Levetiracetam | Subjects who newly visited to the investigator institution during January 1st 2006 to December 31st of 2010 and began their treatment with levetiracetam as mono or add-on therapy with conventional drugs. | ||
| Oxcarbazepine | Subjects who newly visited to the investigator institution during January 1st 2006 to December 31st of 2010 and began their treatment with oxcarbazepine as mono or add-on therapy with conventional drugs. |
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| Measure | Description | Time Frame |
|---|---|---|
| Retention rate of topiramate, levetiracetam and oxcarbazepine during 24 months of treatment | Overall retention rates of three treatment groups at two years will be presented in patient number (% of continuation or discontinuation). | 24months |
| Measure | Description | Time Frame |
|---|---|---|
| Evaluate the confounding factors affecting the retention rate | -Confounding factors associated with retention rate : Seizure Type, gender, age, treatment regimen, number of concomitant medication, type of drug combination, final target dose, titration speed | 24 months |
| Evaluate the response rate through seizure reduction (≥75%, ≥50%) in 2-year treatment with each antiepileptic drugs (topiramate, levetiracetam, oxcarbazepine) |
| Measure | Description | Time Frame |
|---|---|---|
| main reasons of drug discontinuation | 24 months |
Inclusion Criteria:
Exclusion Criteria:
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Subjects who newly visited to epilepsy center in a tertiary hospital during January 1st 2006 to December 31st of 2010
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sang kun Lee, MD, PhD | Contact | sangkun2923@gmail.com | ||
| Jung-won Shin, MD | Contact | limitsum@gmail.com |
| Name | Affiliation | Role |
|---|---|---|
| Sang Kun Lee, MD, PhD | Seoul National University Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Seoul National University Hospital | Recruiting | Seoul | South Korea |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 20633037 | Background | Ramsay E, Faught E, Krumholz A, Naritoku D, Privitera M, Schwarzman L, Mao L, Wiegand F, Hulihan J; CAPSS-272 Study Group. Efficacy, tolerability, and safety of rapid initiation of topiramate versus phenytoin in patients with new-onset epilepsy: a randomized double-blind clinical trial. Epilepsia. 2010 Oct;51(10):1970-7. doi: 10.1111/j.1528-1167.2010.02670.x. | |
| 18616622 |
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| ID | Term |
|---|---|
| D004827 | Epilepsy |
| ID | Term |
|---|---|
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
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| 24 months |
| Peltola J, Peltola M, Auvinen A, Raitanen J, Fallah M, Keranen T. Retention rates of new antiepileptic drugs in localization-related epilepsy: a single-center study. Acta Neurol Scand. 2009 Jan;119(1):55-60. doi: 10.1111/j.1600-0404.2008.01062.x. Epub 2008 Jun 24. |