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Early Detection of Severe Heart Disease in Fetuses at High Risk of Heart Disease

Early Detection of Severe Heart Disease in Fetuses at High Risk of Heart

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04407728
Acronym
PRECAFOET
Enrollment
500
Registered
2020-05-29
Start date
2020-11-15
Completion date
2022-11-02
Last updated
2020-11-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Diseases

Brief summary

The main objective of the work is to evaluate, in the French health care system, the performance of early ultrasound screening for severe heart disease between 11 and 14SA in high-risk populations.

Detailed description

Numerous studies have shown a link between increased nuchal translucency and heart disease. Although high-risk fetal populations are identified between 11 and 13 SA on clinical and biological criteria and by screening ultrasound (Echo T1), cardiac morphology analysis is routinely performed only during 2nd trimester fetal morphology ultrasound between 18 and 22 SA (EchoMorpho-T2) inducing a difficult wait for the couple. The development of increasingly efficient ultrasound probes has made it possible to explore the foetal heart at an earlier stage. International learned societies recommend an early morphological examination with heart-centered slices before 14 weeks in high-risk situations. This practice is not systematic in France and no study has evaluated its feasibility and impact in a French care network.

Interventions

OTHERearly ultrasound screening

Women whose fetus is at high risk of congenital heart disease at the end of the 1st trimester screening ultrasound (EchoT1), will benefit from an early heart-centered morphological ultrasound (EchoMorpho-T1) by a referring sonographer between 11 and 14 SA +/- an early fetal cardiac ultrasound (EchoCoeur-T1) between 11 and 15 SA by a cardio-paediatrician in case of EchoMorpho-T1 abnormality. The results of the early morphological and cardiac ultrasounds will be compared with those of the 2nd trimester ultrasound at 18-22SA (EchoMorpho-T2) and +/- of the fetal cardiac ultrasound between 18SA and 24SA (Gold standard) or, failing this, with the anatomopathological examination when it is available if a medical termination of pregnancy took place before the EchoMorpho-T2.

Sponsors

University Hospital, Grenoble
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Months to No maximum
Healthy volunteers
No

Inclusion criteria

Pregnant women whose fetus is at high risk for congenital heart disease: * Nuchal translucency measurement on T1 echo ≥3.5mm * Cardiac or extra-cardiac morphological abnormality suspected on the T1 screening echo * First degree family history for the fetus (patient, spouse, 1st children of the couple) of significant congenital cardiopathy (excluding AIC, muscular VIC or persistent CA).

Exclusion criteria

* Multiple Pregnancies * non-emancipated minors, persons unable to express their consent. * Lack of affiliation to a social security scheme. * Subject in a period of exclusion from another study, * Subject under administrative or judicial supervision * Subject cannot be contacted in case of emergency

Design outcomes

Primary

MeasureTime frameDescription
early ultrasound screening1 dayCalculation of the sensitivity and specificity of screening for severe heart disease using EchoMorpho-T1. Specificity will be privileged in order to avoid the anxiety-producing nature of false positives.

Contacts

Primary ContactMatthias LACHAUD, PH
MLachaud@chu-grenoble.fr0476769495
Backup ContactLora PEJOT, CRA
LPejot@chu-grenoble.fr0476766561

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026