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A definite syndromic diagnosis, according to the ILAE Classification criteria, ( ) and epilepsies and epileptic syndromes () in epileptic children in a . de la Clasificación Internacional de las Epilepsias y Síndromes Epilépticos en los . Early • In , the ILAE was founded. • In the s, a classification system was purposed by Herni. Gastaut. s. • Anatomy based classification. DOCUMENTOS. CLASIFICACIÓN Y TÉRMINOS EN EPILEPSIA. ILAE Report of the ILAE Classification Core Group. Epilepsia. ILAE Proposal for.

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How to search [pdf]. Clinical trials The European Union Clinical Trials Register allows you to search for protocol and results information on: Clsificacion of the end of the trial and justification where it is not the ilar visit of the last subject undergoing the trial.

Subject is on a ketogenic diet. The trial involves single site in the Member State concerned. A study to assess the safety and efficacy of Lacosamide versus placebo a pill without active medication in patients with idiopathic generalised epilepsy who are already taking anti-epileptic medications.

Cancer AND drug name. Clear advanced search filters. Date on which this record was first entered in the EudraCT database:. Combination product that includes a device, but does not involve an Advanced Therapy.

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Clinical trials

Title of the trial for lay people, in easily understood, i. Regular use of neuroleptics, narcotics, monoamine oxidase MOA inhibitors, barbiturates for indication other than epilepsy within 28 days prior to Visit 1? Women of child bearing potential must practice contraception according to protocol requirements?

Use of Felbamate or Vigabatrin within last 6 months?

Clinical Trials Register

Plans for treatment or care after the subject has ended the participation in the trial if it is different from the expected normal treatment of that condition. Committee on Advanced therapies CAT has issued a classification for this product. Time to the second primary generalized tonic clonic PGTC seizure.

Symptomatic generalized epilepsy, e. Pneumonia AND sponsor name.

Review by the Competent Authority or Ethics Committee in the country concerned. EU Clinical Trials Register. Trials with results Trials without results Clear advanced search filters.

Subjects who choose not to continue in open label study must complete an up to 4-week blinded taper followed by a day Safety Follow-up Period. The IMP has been designated in this indication as an orphan drug in the Community. IMP with orphan designation in the indication. Periodo clasificavion Tratamiento de 24 semanas desde la Visita 2 Semana 0 a la Visita 10 semana To demonstrate the efficacy of oral lacosamide LCM vs placebo as adjunctive therapy for uncontrolled primary generalized tonic-clonic PGTC seizures in subjects with idiopathic generalized epilepsy IGE currently taking 1 to 3 concomitant anti-epileptic drugs AEDs independent of the number of prior failed AEDs.

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Subjects can enter open label study after the completion of Visit 10 Week 24 or End of Treatment Visit and a 4-week blinded transition.

For these items you should use the filters and not add them to clasificacioj search terms in the text field. Trials with results Trials without results. Lifetime history of suicide attempt, or suicidal ideation in past 6 months?

History of partial onset seizures or EEG findings indicating partial onset seizures?

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Las mujeres en edad fertil deben poner iae practivo un metodo anticonceptivo de acuerdo a los requisitos del protocolo. Both Female Only Male Only. Antecedentes de crisis parciales o hallazgos de EEG indicativos de crisis parciales.