Skip to main content
Clinical Trials/NCT06395974
NCT06395974CompletedNot Applicable

Fetal Renal Artery Doppler and Three Dimensional Power Doppler Study of Placenta in Patients With Preeclampsia and Its Role in Prediction of Adverse Neonatal Outcomes

Assiut University2 sites in 1 country114 target enrollmentStarted: November 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
114
Locations
2
Primary Endpoint
fetal renal artery doppler indices

Study Overview

Brief Summary

Preeclampsia is a major devastating disorder affects 2:10% of pregnancies worldwide. preeclampsia may be associated with placental insufficiency which may cause fetal blood redistribution to essential organs like brain, heart, kidney.

Detailed Description

Preeclampsia is a major devastating medical condition that affects pregnant women after 20 weeks of pregnancy. It affects 2:10% of pregnancies worldwide according to World Health Organisation with higher incidence in developing countries.

Vascular endothelial dysfunction due to abnormal placentation is believed to be the main cause of multi-organ failure and uteroplacental insufficiency that occur in preeclampsia leading to major adverse effects in both mother and fetus.

Placental insufficiency causes a redistribution of fetal blood to essential organs ; brain, heart and adrenal glands by decreasing their vascular resistance on expense of peripheral organs. Changes occur in fetal renal circulation in preeclampsia is still area of debate with conflicting results in literature. Doppler ultrasound examination of vasculature of selected organs such as kidneys may have a role in detection of hemodynamic rearrangements that occur in cases of placental insufficiency and preeclampsia.

Also, Three dimensional power Doppler plays a role in comprehensive analysis of placental perfusion. It has a promising results regarding prediction of preeclampsia during early pregnancy and may have insights into prediction of adverse neonatal outcomes in late trimester.

Study Design

Study Type
Observational
Observational Model
Other
Time Perspective
Cross Sectional

Eligibility Criteria

Sex
Female
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • a) Preeclampsia:
  • Women with preeclampsia >28 weeks of pregnancy.
  • Singleton pregnancy.
  • Women with intrauterine growth restriction and abnormal amniotic fluid volume to simulate real world data.
  • b) Control:
  • Women with healthy pregnancy matched by closest gestational age.

Exclusion Criteria

  • ● Multiple pregnancy.
  • Known Congenital fetal malformations.
  • Women with other comorbidity such as ischemic heart disease, DM, Autoimmune disorders, kidney disease, neurological disorders, liver or haematological disorders.
  • Women unable to provide informed consent.
  • Women who refuse to participate

Outcomes

Primary Outcomes

fetal renal artery doppler indices

Time Frame: 1 year

the difference between the Fetal renal artery Doppler indices between preeclamptic patients and women with healthy pregnancy

Middle cerberal artery doppler indices , Umbilical artery doppler indices and placental volume

Time Frame: 1 year

Secondary Outcomes

  • neonatal outcome(1 year)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Yousra M. Othman

principle investigator

Assiut University

Study Sites (2)

Loading locations...

Similar Trials