Hospital
Almaty, Kazakhstan
NCT Number: NCT05121415
To search for a genetic marker of hemorrhagic stroke complicating severe eclampsia, a single nucleotide polymorphism (SNP) analysis of DNA obtained from the peripheral blood of patients with hemorrhagic stroke and normal control will be performed.
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Notify Me18 year–45 year
Female
Observational
Almaty, Kazakhstan
Detailed Description:
Unrelated Korean subjects who have Spontaneous hemorrhagic stroke complicating severe eclampsia in pregnancy were recruited in the current study. Genotyping for various SNP associated due to the linkage disequilibrium patterns is to be performed. Genotypes would be statistically compared between patients with hemorrhagic stroke and normal control subjects free of hemorrhagic stroke
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
-patients with hemorrhagic stroke complicating severe eclampsia in pregnancy
Exclusion criteria
patients without hemorrhagic stroke complicating severe eclampsia in pregnancy
SNP analysis of the DNA obtained from peripheral blood sample
Time frame: 1 year
Asfendiyarov Kazakh National Medical University
Other
Preventive and Personalized Medicine (2021-2023)
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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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