NCT Number: NCT00150774
Levetiracetam as add-on Treatment of Myoclonic Jerks in Adolescents + Adults
A double-blind, placebo-controlled study to assess the efficacy of adjunctive treatment with LEV 3000mg/day in reducing myoclonic seizures in adolescents and adults suffering from idiopathic generalised epilepsy and to evaluate the safety of LEV in the same population.
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Conditions
Age range
12 year–65 year
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Who can participate
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Subjects with a confirmed diagnosis consistent with idiopathic generalized epilepsy experiencing myoclonic seizures (IIB) that are classifiable according to the International Classification of Epileptic Seizures. To ensure an idiopathic generalized epilepsy population, only these subjects with the diagnosis of juvenile myoclonic epilepsy (JME), juvenile absence epilepsy (JAE) or epilepsy with generalized tonic- clonic seizures on awakening must be included.
- Presence of at least eight days with at least one myoclonic seizure (IIB) per day during the eight weeks of the Baseline period.
- Absence of brain lesion documented on a CT scan or MRI; if a CT scan or MRI has not been performed within the past five years before Visit 1, a CT scan (or MRI where legally required) should be performed during the Baseline period.
- Presence of EEG features consistent with idiopathic generalized epilepsy on an EEG recorded during the Baseline period or no more than one year before Visit 1.
- Male/female children ≥ 12 years of age or adult ≤ 65 years of age at Visit 1.
- Subject on a stable dose of one standard anti-epileptic treatment for at least four weeks before Visit 1.
Exclusion criteria
- Previous exposure to levetiracetam.
- History of partial seizures.
- History of convulsive or non-convulsive status epilepticus within 3 months prior to Visit 1.
- Subject taking vigabatrin or tiagabine, subject on felbamate with less than 18 months exposure, and subject under vagal nerve stimulation or ketogenic diet.
- Subject taking any drug (except the concomitant AEDs) with possible CNS effects.
Treatment and study plan
Primary outcomes
-
Responder rate in myoclonic (type IIB) seizures days over 16 weeks
Secondary outcomes
-
Safety and tolerability of levetiracetam by means of AE, laboratory assessments, plasma concentration
Sponsors and collaborators
Lead sponsor
UCB Pharma
Industry
Registry information
Official study title
A Double-blind, Multicenter, Randomized, Placebo-controlled Study to Evaluate the Efficacy and Safety of Levetiracetam (LEV) (Oral Tablets of 500 mg b.i.d.) at a Dose of 3000 mg/Day as Adjunctive Treatment in Adolescents (≥ 12 Years) and Adults (≤ 65 Years) Suffering From Idiopathic Generalized Epilepsy With Myoclonic Seizures.
Important dates
- Study start
- 2001
- Primary completion
- 2004
- Study completion
- 2004
- First posted
- Sep 8, 2005
- Registry last updated
- Sep 17, 2013
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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