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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
University Hospital, Grenoble
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Heart Diseases

Eligibility Criteria

18 Months - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

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

    First Posted
    May 25, 2020
    Last Updated
    November 4, 2020
    Sponsor
    University Hospital, Grenoble
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    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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