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

NCT04368936 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 121

Last updated 2021-10-19

No results posted yet for this study

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.

Conditions

  • Febrile Seizure

Interventions

GENETIC

Isolated DNA, Real Time PCR

We are isolated DNA from the blood sample. To determine the genotypes of the analyzed polymorphisms use real-time PCR using TaqMan essays. When analyzing the KCC2 polymorphisms, the VIC dye gene corresponded to the C allele, and the FAM dye corresponded to the T allele, while at the TRPV1 gene polymorphism, the VIC dye corresponded to the C allele and the FAM dye to the G allele.

Sponsors & Collaborators

  • Institut za Rehabilitaciju Sokobanjska Beograd

    lead OTHER

Principal Investigators

  • Sanja Dimitrijevic, PhD · Specila hospital for cerebral palsy and developmental neurology

Eligibility

Min Age
1 Year
Max Age
14 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-03-31
Primary Completion
2019-05-15
Completion
2021-08-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04368936 on ClinicalTrials.gov