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

Asfendiyarov Kazakh National Medical University100 enrolled

Overview

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: 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 Type

OBSERVATIONAL

Enrollment

100

Conditions

Hemorrhagic Stroke Eclampsia

Interventions

SNP analysis of the DNAGENETIC

SNP analysis of the DNA obtained from peripheral blood sample

Eligibility

Sex: FEMALEMin age: 18 YearsMax age: 45 Years

Medical Language ↔ Plain English

Inclusion Criteria: -patients with hemorrhagic stroke complicating severe eclampsia in pregnancy Exclusion Criteria: patients without hemorrhagic stroke complicating severe eclampsia in pregnancy

Locations (1)

Hospital

Almaty, Kazakhstan

Outcomes

Primary Outcomes

genotyping for the SNP associated with hemorrhagic stroke complicating severe eclampsia in pregnancy

Time frame: 1 year

Data from ClinicalTrials.gov

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