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Clinical-genetic Investigations in Children With Early Infantile Epilepsies

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ClinicalTrials.gov Identifier: NCT01357707
Recruitment Status : Completed
First Posted : May 23, 2011
Last Update Posted : February 12, 2018
Sponsor:
Collaborators:
Mainz University
University of Ulm
Ludwig-Maximilians - University of Munich
University of Kiel
Information provided by (Responsible Party):
Markus Schuelke, M.D., Charite University, Berlin, Germany

Brief Summary:

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.


Condition or disease Intervention/treatment
Epilepsy Seizures, Infantile Genetic: DNA preparation

Study Type : Observational
Actual Enrollment : 75 participants
Observational Model: Family-Based
Time Perspective: Prospective
Official Title: Clinical-genetic Investigations in Children With Early Infantile Epilepsies
Study Start Date : July 2010
Actual Primary Completion Date : December 31, 2017
Actual Study Completion Date : December 31, 2017

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Epilepsy Seizures

Group/Cohort Intervention/treatment
West Syndrome (idiopathic)
Patients with idiopathic infantile seizures
Genetic: DNA preparation
Taking blood or saliva from the patient to prepare DNA therefrom




Primary Outcome Measures :
  1. Discovery of a pathogenic mutation in an ion channel gene [ Time Frame: 4 weeks after taking of the DNA specimen ]

Biospecimen Retention:   Samples With DNA
DNA isolated from blood cells or from saliva


Information from the National Library of Medicine

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Ages Eligible for Study:   5 Years to 10 Years   (Child)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients with infantile seizures without brain malformations, metabolic disorders of lissencephaly who had a good outcome and are seizure free (with or without AEDs) after the age of 5 years.
Criteria

Inclusion Criteria:

  • Hypsarrhythmia in the first year of life
  • Infantile seizures in the first year of life
  • Freedom of seizures at the age of 5 years

Exclusion Criteria:

  • brain malformation
  • metabolic disorder
  • intracranial hemorrhage
  • lissencephaly

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01357707


Locations
Germany
Charité Universitätsmedizin
Berlin, Germany, 13353
Sponsors and Collaborators
Markus Schuelke, M.D.
Mainz University
University of Ulm
Ludwig-Maximilians - University of Munich
University of Kiel

Responsible Party: Markus Schuelke, M.D., Prinicpal investigator, Charite University, Berlin, Germany
ClinicalTrials.gov Identifier: NCT01357707     History of Changes
Other Study ID Numbers: EA1_215_08
SFB 665 TP C4 ( Other Grant/Funding Number: Deutsche Forschungsgemeinschaft )
First Posted: May 23, 2011    Key Record Dates
Last Update Posted: February 12, 2018
Last Verified: February 2018

Additional relevant MeSH terms:
Epilepsy
Seizures
Brain Diseases
Central Nervous System Diseases
Nervous System Diseases
Neurologic Manifestations
Signs and Symptoms