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Blood Markers of Blood Vessel Activation in Pregnancies With High Blood Pressure

Compares blood vesicle markers in pregnant adults with and without high blood pressure disorders.

Plain-language title generated from the registry record
Registry title: Endothelial Extracellular Vesicles as Biomarkers of Endothelial Activation in Pregnant Women With Hypertensive Disorders of Pregnancy

Key facts

Where
Osijek, CroatiaSee the site

AI summary: who the study is looking for

From the trial's eligibility criteria. Machine-read from the registry text on this page, so it can be wrong. The registry text below and the trial team decide who can take part.

The trial is looking for pregnant women aged 18 or older with a single baby. Some have normal blood pressure, and some have high blood pressure caused by pregnancy.

Age
18 years or older
Sex
Female only (pregnant women)
Disease stage
Either a normal-blood-pressure pregnancy, or gestational hypertension or preeclampsia diagnosed by current clinical guidelines.

Main reasons for not taking part

  • High blood pressure that began before pregnancy
  • Pregnancy with more than one baby
  • Diabetes before pregnancy
  • Chronic kidney disease
  • Autoimmune disease, known heart or blood vessel disease, active infection or inflammatory disease, or cancer

This trial only enrols pregnant participants. The registry sentence this rests on: Pregnant women aged ≥18 years.

Read by machine on 9 November 2026.

Where in Croatia

  • Faculty of Medicine OsijekOsijek, CroatiaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?

Contact the study team: see the registry record → Contacts and Locations

Print a page for my doctor

Trial details

Who runs it
Josip Juraj Strossmayer University of Osijek
Trial code
NCT07728656
Record updated
27 July 2026
Original description
Hypertensive disorders of pregnancy are associated with endothelial dysfunction and increased maternal and fetal morbidity. Endothelial extracellular vesicles (EEVs) have emerged as promising biomarkers of endothelial activation; however, their relationship with blood pressure and endothelial function during pregnancy remains incompletely understood. This observational case-control study aims to compare circulating EEV concentrations between normotensive pregnant women and pregnant women with hypertensive disorders of pregnancy. The study will also investigate the associations between EEV levels, blood pressure, microvascular endothelial function assessed by laser Doppler flowmetry, and circulating biomarkers of endothelial activation. The findings may improve understanding of endothelial injury during pregnancy and support the development of non-invasive biomarkers for early detection and monitoring of hypertensive disorders of pregnancy.Read full original descriptionShow less

Endothelial Extracellular Vesicles as Biomarkers of Blood Pressure-Induced Endothelial Activation in Pregnant Women With Hypertensive Disorders of Pregnancy

Hypertensive disorders of pregnancy are associated with endothelial dysfunction and increased maternal and fetal morbidity. Endothelial extracellular vesicles (EEVs) have emerged as promising biomarkers of endothelial activation; however, their relationship with blood pressure and endothelial function during pregnancy remains incompletely understood. This observational case-control study aims to compare circulating EEV concentrations between normotensive pregnant women and pregnant women with hypertensive disorders of pregnancy. The study will also investigate the associations between EEV levels, blood pressure, microvascular endothelial function assessed by laser Doppler flowmetry, and circulating biomarkers of endothelial activation. The findings may improve understanding of endothelial injury during pregnancy and support the development of non-invasive biomarkers for early detection and monitoring of hypertensive disorders of pregnancy.

Inclusion: Pregnant women aged ≥18 years; Singleton pregnancy; Ability to provide written informed consent; Normotensive pregnancy or diagnosis of gestational hypertension or preeclampsia according to current clinical guidelines; Ability to comply with study procedures.

Exclusion: Chronic hypertension diagnosed before pregnancy; Pre-existing diabetes mellitus; Chronic kidney disease; Autoimmune disease; Known cardiovascular disease; Active infection or inflammatory disease; Malignancy; Multiple pregnancy; Inability or unwillingness to provide informed consent.

ClinicalTrials.gov NCT07728656