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Investigation of Genetic Disease Marker Associated With Spontaneous Haemorrhagic Stroke Complicating Severe Pre-eclampsia in Pregnancy

Hemorrhagic Stroke Clinical Trial

Official title:
Preventive and Personalized Medicine (2021-2023)

Clinical Trial Summary

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.

Clinical Trial Description

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 ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05121415
Study type Observational
Source Asfendiyarov Kazakh National Medical University
Contact
Status Completed
Phase
Start date October 23, 2021
Completion date January 20, 2023
View Details
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