CompletedNot Applicable

Relationship Between Polymorphisms of TRPV1 and KCC2 Gene in Children With Febrile Seizures

121 participantsStarted 2015-03-31

Plain-language summary

Febrile seizures (FS) are the most common neurological disorder in chilhood. The etiology of FN is still the subject of numerous studies and it is known that it can depend on genetic predisposition.

Who can participate

Age range1 Year – 14 Years

SexALL

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Inclusion Criteria: * Our research involve patient with diagnosed Febrile Seizure which were hospitalized or recieved ambulatory treatment in University Children´s Hospital in Belgrade * For each patient, a diagnosis of FS was made based on the ILAE definition (International Leage * The main criterion for inclusion in the study was enhanced FS without prior occurrence of afebrile seizure. Exclusion Criteria: * Patients with evidence of intracranial infections and metabolic disbalance * Patients with incomplited medical documentation

What they're measuring

Detection of the polymorphism in the TRPV1 gene polymorphisms

Timeframe: 2 weeks

Detection of the polymorphism in the KCC2 gene polymorphisms

Timeframe: 2 weeks

Trial details

NCT IDNCT04368936

SponsorInstitut za Rehabilitaciju Sokobanjska Beograd

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2019-05-15

View on ClinicalTrials.gov More Febrile Seizure trials