ClinConnect ClinConnect Logo
Search / Trial NCT05284474

Management of Early-onset Fetal Growth Restriction: Angiogenic Factors Versus Feto-placental Doppler

Launched by HOSPITAL UNIVERSITARI VALL D'HEBRON RESEARCH INSTITUTE · Mar 9, 2022

Trial Information

Current as of May 05, 2025

Not yet recruiting

Keywords

Fetal Growth Restriction Small For Gestational Age Pl Gf S Flt 1 Doppler

ClinConnect Summary

This clinical trial is exploring how to manage early-onset fetal growth restriction, a condition where a baby is not growing as expected during pregnancy. The study will involve 340 pregnant women who are between 26 and 31 weeks along and have a measured fetal weight that is smaller than normal (less than the 10th percentile). Participants will be randomly assigned to one of two groups: one group will receive standard care based on ultrasound blood flow measurements (Doppler), while the other group will use a new method that involves specific blood test results to help decide how often ultrasounds are done and when to plan for delivery.

To be eligible for this trial, women must be at least 18 years old and have a single baby (not twins or more) with a low fetal weight during the specified weeks of pregnancy. They should also have a confirmed gestational age from an early pregnancy scan or from fertility treatment. Unfortunately, women with serious fetal problems or who are not willing to participate cannot join the study. This trial is not yet recruiting participants but aims to find better ways to care for pregnancies affected by growth issues.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Pregnant women of at least 18 years old
  • Singleton pregnancy
  • Ultrasonographic EFW ≤10th percentile between 26+0 and 31+6 weeks of gestation
  • Gestational age confirmed by fetal crown-rump length measurement during the first trimester scan (from 11+0 to 13+6 weeks of gestation) or by in vitro fertilization dates.
  • Exclusion Criteria:
  • Major fetal malformations or genetic disorders
  • Fetal death
  • Refusal to give informed consent
  • Stage IV FGR

About Hospital Universitari Vall D'hebron Research Institute

The Hospital Universitari Vall d'Hebron Research Institute (VHIR) is a leading biomedical research center affiliated with Vall d'Hebron University Hospital in Barcelona, Spain. Committed to advancing healthcare through innovative research, VHIR focuses on translating scientific discoveries into clinical applications, enhancing patient care and outcomes. The institute fosters collaboration among multidisciplinary teams of researchers, clinicians, and industry partners, emphasizing excellence in translational medicine, clinical trials, and public health initiatives. With a strong emphasis on ethical standards and patient safety, VHIR is dedicated to contributing to the global body of knowledge in various medical fields.

Locations

Madrid, , Spain

Barcelona, , Spain

Zaragoza, , Spain

Lleida, , Spain

Elche, , Spain

Getafe, , Spain

Badalona, , Spain

Santa Cruz De Tenerife, , Spain

Cadiz, , Spain

Palma De Mallorca, , Spain

Lleida, , Spain

Terrassa, , Spain

Sevilla, , Spain

Granada, , Spain

Girona, , Spain

Barcelona, , Spain

A Coruña, , Spain

Sabadell, , Spain

Tarragona, , Spain

Gijón, , Spain

Jerez De La Frontera, , Spain

Barcelona, , Spain

Alicante, , Spain

Terrassa, , Spain

Torrejón De Ardoz, , Spain

Palma De Mallorca, , Spain

Las Palmas De Gran Canaria, , Spain

Sevilla, , Spain

Patients applied

0 patients applied

Trial Officials

Manel Mendoza, MD, PhD

Principal Investigator

Vall d'Hebron Institut de Recerca (VHIR)

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Similar Trials