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OpenTrials
Completed

NCT Number: NCT05088499

The Role of Genetic Factors in the Development of Epilepsy in the Kazakh Population

This is a GWAS study that aims to identify possible candidate genes associate to epilepsy by exploring single nucleotide polymorphism (SNP) in a group of epilepsy, in the Kazakh population. The investigators hypothesize that the careful phenotyping of the subject sand matching with increase the power to find SNP significantly associate with epilepsy

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Key information

Age range

0 year–5 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Altynshash Jaxybayeva

Almaty, Kazakhstan

About this study

A genome-wide association study (GWAS) is an approach used in genetics research to associate specific genetic variations with particular diseases. The method involves scanning the genomes from many different people and looking for genetic markers that can be used to predict the presence of a disease. Once such genetic markers are identified, they can be used to understand how genes contribute to the disease and develop better prevention and treatment strategies

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children with seizures, confirmed by EEG and no morphological damage to the brain, confirmed by MRI of the brain;
  • The age of the patients is from 0 to 5 years;
  • Persons of Kazakh nationality, whose paternal and maternal grandparents are Kazakhs;
  • Children are parents or legal guardians who have given written informed consent.

Exclusion criteria

  • Children over 5 years old;
  • Children whose parents, according to the researcher, are mentally or legally incapacitated, which prevents obtaining informed consent;
  • Children with seizures with brain damage that cause epilepsy;
  • Children of a non-Kazakh ethnic group.

Treatment and study plan

DNA analysis

Genetic

GWAS

Primary outcomes

  1. number of SNPs associated with epilepsy

    Time frame: 1 year

    Using GWAS to identify candidate genes associate with epilepsy

Sponsors and collaborators

Lead sponsor

Asfendiyarov Kazakh National Medical University

Other

Registry information

Official study title

Preventive and Personalized Medicine (2021-2023)

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Oct 22, 2021
Registry last updated
Mar 14, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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