Early Detection of Severe Heart Disease in Fetuses at High Risk of Heart Disease (PRECAFOET)
Primary Purpose
Heart Diseases
Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
early ultrasound screening
Sponsored by
About this trial
This is an interventional diagnostic trial for Heart Diseases
Eligibility Criteria
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
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
precocious EchoMorpho-T1
Arm Description
Women whose fetus is at high risk of congenital heart disease after the 1st trimester screening echo (EchoT1), will benefit from an early morphological ultrasound centered on the heart (EchoMorpho-T1) by a sonographer referent between 11 and 14 weeks +/- of an early fetal heart ultrasound (EchoCoeur-T1) between 11 and 15 weeks by a cardio-pediatrician in the event of an abnormality with the EchoMorpho-T1.
Outcomes
Primary Outcome Measures
early ultrasound screening
Calculation 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.
Secondary Outcome Measures
Full Information
NCT ID
NCT04407728
First Posted
May 25, 2020
Last Updated
November 4, 2020
Sponsor
University Hospital, Grenoble
1. Study Identification
Unique Protocol Identification Number
NCT04407728
Brief Title
Early Detection of Severe Heart Disease in Fetuses at High Risk of Heart Disease
Acronym
PRECAFOET
Official Title
Early Detection of Severe Heart Disease in Fetuses at High Risk of Heart
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
November 15, 2020 (Anticipated)
Primary Completion Date
May 2, 2022 (Anticipated)
Study Completion Date
November 2, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Grenoble
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Diseases
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
500 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
precocious EchoMorpho-T1
Arm Type
Experimental
Arm Description
Women whose fetus is at high risk of congenital heart disease after the 1st trimester screening echo (EchoT1), will benefit from an early morphological ultrasound centered on the heart (EchoMorpho-T1) by a sonographer referent between 11 and 14 weeks +/- of an early fetal heart ultrasound (EchoCoeur-T1) between 11 and 15 weeks by a cardio-pediatrician in the event of an abnormality with the EchoMorpho-T1.
Intervention Type
Other
Intervention Name(s)
early ultrasound screening
Intervention Description
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.
Primary Outcome Measure Information:
Title
early ultrasound screening
Description
Calculation 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.
Time Frame
1 day
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Matthias LACHAUD, PH
Phone
0476769495
Ext
+ 33
Email
MLachaud@chu-grenoble.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Lora PEJOT, CRA
Phone
0476766561
Ext
+33
Email
LPejot@chu-grenoble.fr
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Early Detection of Severe Heart Disease in Fetuses at High Risk of Heart Disease
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