CLASIFICACION ILAE 1981 PDF

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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Clinical trials The European Union Clinical Trials Register allows you to search for protocol and results information on: Cancer AND drug name. Pneumonia AND sponsor name. How to search [pdf].

For these items you should use the filters and not add them to your search terms in the text field. Trials with results Trials without results Clear advanced search filters. Review by the Competent Authority or Ethics Clasifocacion in the country concerned. EU Clinical Trials Register. Both Female Only Male Only. IMP with orphan designation in the indication.

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Trials with results Trials without results. Clear advanced search filters. Date on which this record was first entered in the EudraCT database:.

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Title of the trial for lay people, in easily understood, i. 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.

Clinical Trials Register

The IMP has been designated in this indication as an orphan drug in the Community. Committee on Advanced therapies CAT has issued a classification for this product. Combination product that includes a device, but does not involve an Advanced Therapy.

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.

History of partial onset seizures or EEG findings indicating partial onset seizures? Symptomatic generalized epilepsy, e. Lifetime history of suicide attempt, or suicidal ideation in past 6 months?

Clinical trials

Women of child bearing potential must practice contraception according to protocol requirements? Regular use of neuroleptics, narcotics, monoamine oxidase MOA inhibitors, barbiturates for indication other than epilepsy within 28 days prior to Visit 1?

Use of Felbamate or Vigabatrin within last 6 months? Ilar is on a ketogenic diet.

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

Time to the second primary generalized tonic clonic PGTC seizure. Periodo de Tratamiento de 24 semanas desde clasivicacion Visita 2 Semana 0 a la Visita 10 semana The trial involves single site in the Member State concerned. Definition of the end of the trial and justification where it is not the last visit of the last subject undergoing the trial.

Plans for treatment or care after the subject has ended the participation in clasificacioon trial if it is different from the expected normal treatment of that condition. 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.

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.