Status:
COMPLETED
Relationship Between Polymorphisms of TRPV1 and KCC2 Gene in Children With Febrile Seizures
Lead Sponsor:
Institut za Rehabilitaciju Sokobanjska Beograd
Conditions:
Febrile Seizure
Eligibility:
All Genders
1-14 years
Brief 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.
Detailed Description
Febrile seizures (FS) are the most common neurological disorder in chilhood. It is precisely because of the high incidence of the disease, the age that includes the tendency of repetition, represent a...
Eligibility Criteria
Inclusion
- 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
- Patients with evidence of intracranial infections and metabolic disbalance
- Patients with incomplited medical documentation
Key Trial Info
Start Date :
March 31 2015
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
August 1 2021
Estimated Enrollment :
121 Patients enrolled
Trial Details
Trial ID
NCT04368936
Start Date
March 31 2015
End Date
August 1 2021
Last Update
October 19 2021
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