Ireland
--:--IST
Recruiting Observational

Selective Fetal Growth Restriction in Monochorionic Twins - an International Investigation

NCT05952583 · tracked via the Priya Life Science Spain tracker
Phase
Observational
Started
2023-02-17
Last updated
2024-04-15

Condition(s) studied

Twin; Pregnancy, Affecting Fetus or NewbornFetal Growth RetardationTwin Monochorionic Diamniotic PlacentaTwin Diseases

Investigational drug(s) / intervention(s)

Ultrasound

Ultrasound: Additional ultrasound measurements during pregnancy

Study summary

Optimal diagnostic management and underlying pathophysiological mechanisms of selective fetal growth restriction (sFGR) in monochorionic diamniotic (MCDA) twin pregnancies have not been fully clarified.

The current diagnostic classification system based on three different umbilical artery flow patterns has no increasing scale of severity and the predictive value is limited. Since there is no treatment available for sFGR, predicting fetal deterioration is key in preventing single or double fetal demise. Outcome prediction is furthermore important in the selection of cases that will be offered selective reduction (to provide the larger twin with better prospects), as well as determining monitor frequency and possible hospital admission. As outcome prediction is clinically challenging, patient counselling is too, and parents often encounter a great deal of uncertainty during the pregnancy.

Furthermore, little is known about the brain development of sFGR children (both during pregnancy and after birth). Moreover, the psychological impact of an sFGR pregnancy of the future parent)s) has not been studied before. The impact of these factors should be taken into account during patient counseling, which is currently not the case.

By our knowledge, this is the first international, multicenter, prospective cohort study on that will address the abovementioned questions and knowledge gaps in MCDA pregnancies complicated by selective fetal growth restriction.

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: * MCDA twin pregnancy * Diagnosis of sFGR before 28+0 weeks of GA (independent of Doppler flows) * Pregnant woman ≥ 18 years and able to consent * Partner (who has (future) parental responsibility - if applicable) ≥ 18 years and able to consent * Written informed consent of both parents (if applicable) for participation in the longitudinal follow-up until 2 years after birth) Exclusion Criteria: * The presence of lethal anomalies (one or both fetuses) * Multiple pregnancy higher order than twins; * TTTS/TAPS present at moment of sFGR diagnosis.

Primary outcome measure(s)

  • Composite outcome — 2 years
    The composite outcome consists of fetal single or double demise, including selective fetal reduction and/or an iatrogenic elective birth \< 32 weeks of gestational age because of fetal distress).

Trial sites (6)

FacilityCityRegionStatus
Boston Children's Hospital Boston Massachusetts Recruiting
Universitaire Ziekenhuizen Leuven Leuven Belgium Recruiting
Mount Sinai Hospital Toronto Ontario Recruiting
Leiden University Medical Center Leiden South Holland Recruiting
BCNatal Barcelona Spain Recruiting
Karolinska University Hospital Stockholm Sweden Not Yet Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05952583 on ClinicalTrials.gov ↗ ← All trials in Spain