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Completed

NCT Number: NCT06712550

Assessment of Maternal and Fetal Serum Biomarkers in Women With Pre-eclampsia

The findings of markers of placental dysfunction in women with preeclampsia may suggest that these biomarkers may be useful tools for early detection of preeclampsia

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Observational

Primary location

Hawler Medical University

Erbil, Kurdistan Region, 44001, Iraq

About this study

Preeclampsia is a pregnancy-specific hypertension illness that is characterized by widespread maternal endothelial dysfunction and appears to be a systemic syndrome that originates in the placenta. Through binding to and blocking the interaction of placental growth factor (PlGF) and vascular endothelial growth factor (VEGF) with their receptors Flt1, soluble fms-like tyrosine kinase (sFlt1) functions as an antagonist of these growth factors. Most seromucoid and protein-bound hexose are released during an acute phase and are inflammatory glycoproteins. Hepatocytes in the liver, which are highly sensitive to stress, increase and leak into the bloodstream during any disease state. It is a time when the placenta demands more vascular development. In order to identify and explain the differences in sFLT-1, VEGF, PlGF levels, and inflammatory biomarker responses. Current study will investigate the differences in blood level of sFLT-1, VEGF, PLGF, Seromucoid and protein-bound hexose inflammatory biomarkers between those with PE (cases) and healthy pregnant women (controls).

Who can participate

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

Inclusion criteria

  • Age group 18-45 years
  • Gestational age of 26-41 weeks at the time of diagnosis for preeclampsia
  • Delivered vaginally or abdominally
  • Being of any parity (para 1 and more)
  • Pregnancy being singleton or multiple pregnancies
  • Willingness to provide informed consent

Exclusion criteria

  • Pregnant woman having chronic hypertension
  • Having Diabetes mellitus
  • The lady on medications that can affect inflammatory markers or blood pressure
  • Pregnant with fetal anomalies
  • Refused to involve in the research

Treatment and study plan

Primary outcomes

  1. To compare the levels of maternal and fetal serum soluble Fms-like tyrosine kinase-1 (sFlt-1), seromucoid, and protein-bound hexose between women with pre-eclampsia and a control group of healthy pregnant women.

    Time frame: one hour

    To quantify and compare the concentrations of soluble Fms-like tyrosine kinase-1 (sFlt-1), seromucoid, and protein-bound hexose in maternal and fetal serum between women diagnosed with pre-eclampsia and a control group of normotensive pregnant women.

Secondary outcomes

  1. To assess the association between the levels of these biomarkers and the severity of pre-eclampsia.

    Time frame: one hour

    o quantify and compare the concentrations of soluble Fms-like tyrosine kinase-1 (sFlt-1), seromucoid, and protein-bound hexose in maternal and fetal serum between women diagnosed with pre-eclampsia and a control group of normotensive pregnant women.

Sponsors and collaborators

Lead sponsor

SHAHLA KAREEM ALALAF

Other

Registry information

Official study title

Assessment of Maternal and Fetal Serum Soluble Fms-like Tyrosine Kinase-1, Seromucoid, and Protein-bound Hexose in Women With Pre-eclampsia: A Case-control Study

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Dec 2, 2024
Registry last updated
Jul 16, 2025

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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