NCT05121415

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

Preventive and Personalized Medicine (2021-2023)

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 100 (actual)
• Sponsor: Asfendiyarov Kazakh National Medical University · Academic / Other
• Sex: Female
• Age: 18 Years – 45 Years
• Healthy volunteers: —

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.

Detailed 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

Conditions

• Hemorrhagic Stroke
• Eclampsia

Interventions

Type	Name	Description
GENETIC	SNP analysis of the DNA	SNP analysis of the DNA obtained from peripheral blood sample

Timeline

• Start date: 2021-10-23
• Primary completion: 2023-01-20
• Completion: 2023-01-20
• First posted: 2021-11-16
• Last updated: 2023-03-14

Locations

1 site across 1 country: Kazakhstan