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Epilepsy clinical trials

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NCT ID: NCT01376180 Completed - Epilepsy Clinical Trials

Drug Use Investigation for LAMICTAL

Start date: December 2008
Phase: N/A
Study type: Observational

The purpose of this study is to grasp actual status of usage of lamotrigine tablet and to collect information for using lamotrigine tablet effectively and safely as well as to grasp onset status of adverse events in pediatric subjects, geriatric subjects, pregnant women, subjects with poor renal and hepatic functions.

NCT ID: NCT01374204 Completed - Epilepsy Clinical Trials

Epilepsy-Associated Stigma

EPISTIGMA
Start date: July 2011
Phase:
Study type: Observational

Few data about epilepsy-associated stigma in France are available. The only study we have found showed that in France 66% of people with epilepsy felt stigmatized by their condition and are often single, compared with the other European patients interviewed (Baker et al., 2000). The purpose of this study is to assess the association between type of epilepsy (drug resistant-epilepsy and stabilized epilepsy) and perceived stigma (using the Stigma Scale) in patients recruited in the Limousin region .

NCT ID: NCT01373190 Completed - Partial Epilepsy Clinical Trials

Thermographic Examination of Skin Temperatures in Individuals With Focal Onset Epilepsy

Start date: May 2011
Phase: N/A
Study type: Observational

The specific aim is to determine if there are patterns of temperature differences in the abdominal and back regions of individuals with partial/focal onset epilepsy as compared to a non-epileptic control group. The hypothesis is that individuals with partial/focal onset epilepsy will have colder recorded temperatures in the abdominal area than individuals in a matched control group.

NCT ID: NCT01364597 Completed - Epilepsy Clinical Trials

Open-label Long-term Study of Adjunctive Brivaracetam in Pediatric Subjects With Epilepsy

Start date: August 1, 2011
Phase: Phase 3
Study type: Interventional

This study will evaluate the safety and tolerability of brivaracetam in pediatric subjects with epilepsy.

NCT ID: NCT01364558 Completed - Epilepsy Clinical Trials

A Study of Diazepam After Intranasal and Intravenous Administration to Healthy Volunteers

Start date: February 2011
Phase: Phase 1
Study type: Interventional

The purpose of this clinical research study is to assess the bioavailability and pharmacokinetics of two formulations of diazepam after intranasal (nasal spray) and injectable diazepam after intravenous (I.V.) administration

NCT ID: NCT01363154 Terminated - Epilepsy Clinical Trials

Prevention of Photoparoxysmal Abnormalities by Mozart K448

Start date: November 2010
Phase: N/A
Study type: Interventional

The purpose of this clinical trial is to examine the effect of non-invasive cortical activation by specific patterned auditory stimulation (Mozart K448- Piano Sonata for Two Hands in D Major), in altering or eliminating photoparoxysmal abnormalities. Recent work has indicated that such evoked activity (i.e. by specific music) can result in significant reductions, or even complete termination of epileptiform activity and/or seizures across a broad range of individuals with epilepsy. A hypothesis is generated that specific music activation would beneficially effect photoparoxysmal based epileptiform abnormalities.

NCT ID: NCT01357902 Completed - Epilepsy Clinical Trials

Lamotrigine Bioequivalence Study to Compare Dispersible Tables With Compressed Tablets in China

Start date: April 18, 2011
Phase: Phase 1
Study type: Interventional

It is an open-label, randomised, single dose, two-sequence cross-over study. Twenty-four eligible, healthy, Chinese male subjects will be enrolled after providing written informed consent. Subjects will be randomised into two treatment groups 1 day prior to the first dosing day and will be assigned to regimen sequences (AB or BA) in a balanced fashion in accordance with the randomisation schedule. Regimen A is five lamotrigine 5 mg chewable/dispersible tablets and Regimen B is one lamotrigine 25 mg standard/compressed tablet. Subjects will receive their allocated regimen on the morning of Day 1 and will undergo study assessments for 7 days (until Day 8). Subjects will receive their alternate randomised treatment after a washout period of 14-21 days from Day 1. Subjects will undergo a further assessment period of 7 days and will attend a follow-up visit during 8-12 days after the second treatment. The total observation period in this study will be 23~34 days. Subjects will arrive at the research unit on the evening before each lamotrigine dosing occasion and will remain in the unit until the 24-h post-dose evaluations have been completed (pre-dose, 0.5, 1, 1.5, 2, 2.5, 3, 4, 6, 8, 12 and 24 h). After this, subjects will return home but must return to the unit for further assessments to be made at 36, 48, 72, 96, 120, 144 and 168 h after dosing Study Endpoints/Assessments A total of 19 serial blood samples (5 mL each) will be collected for the measurement of plasma lamotrigine concentrations at each study assessment. Safety and tolerability assessments (monitoring of adverse events and serious adverse events, routine laboratory determinations, vital sign measurements and 12-lead electrocardiogram) will be conducted throughout the study.

NCT ID: NCT01357707 Completed - Epilepsy Clinical Trials

Clinical-genetic Investigations in Children With Early Infantile Epilepsies

Start date: July 2010
Phase: N/A
Study type: Observational

The project strives to discover novel genetic defects that cause monogenic epilepsy or that genetically modify a preexisting epileptic phenotype. Our main aim is to find genetic causes for the idiopathic West Syndrome (infantile seizures) that are not caused by known cerebral malformation, lissencephaly or metabolic disorders and which have a comparatively benign prognosis. The investigators hypothesize that mutations in genes coding for ion channels or genes that modify the action of ion channels might be causative. For that the investigators will perform a sequence analysis of the coding exons of a large set of genes in all recruited patients and verify found mutations in their parents.

NCT ID: NCT01355211 Completed - Clinical trials for Altered Mental Status

Putting Electroencephalography (EEG) in the Emergency Department

Start date: April 2011
Phase: N/A
Study type: Observational

The aim of the proposed research is to compare the diagnostic accuracy of a portable wireless electroencephalography (EEG) device (Biosignal Micro-EEG) to standard EEG in identifying abnormal EEG patterns (mainly non-convulsive seizure and non-convulsive status epilepticus) in emergency department (ED) patients with altered mental status. Comparing the the accuracy of EEG recordings and interpretations of Micro-EEG to those of standard EEG will allow the investigators to assess the utility of this novel device in the ED patients with altered mental status. The unique qualities of Micro-EEG device could potentially facilitate easier access to EEG test in all ED patients. This study will also provide valid information regarding the prevalence of non-convulsive seizure in ED patients with altered mental status.The gold standard for diagnosing non-convulsive seizure would be standard EEG. All study participants will undergo electroencephalography using the two devices (standard EEG and micro-EEG) and a combination of standard electrodes and Electro-Cap in a randomized order: 1. Standard EEG with standard EEG electrodes, 2. Micro-EEG with standard EEG electrodes, and 3. Micro-EEG with Electro-Cap electrodes.

NCT ID: NCT01351727 Completed - Epileptic Seizures Clinical Trials

Epidemiologic Follow Up Study of Newly Diagnosed Epilepsy Among Seniors

Start date: January 2011
Phase: N/A
Study type: Observational

The purpose of this proposed research is to identify individuals in southeastern Arizona aged 65 years and older who have new onset seizures (or newly diagnosed epilepsy) and monitor them for at least two years. In doing so the investigators will be able to describe the public health burden of this condition and to identify factors that predict clinical outcomes and health care needs in this population, using quantitative, administrative, and qualitative data. The aims of this proposed research are 1) to determine the two-year incidence of newly diagnosed epilepsy in the target population, 2) describe health care resource utilization of the target population using Medicare data, 3) validate the use of Medicare beneficiary data to estimate incidence of epilepsy, and 4) describe the burden of this condition in different ethnic groups.