Could a simple DNA test predict SIDS risk? new study hopes to find out

NCT ID NCT06244433

First seen May 12, 2026 · Last updated May 12, 2026

Summary

This study aims to find genetic changes that may increase the risk of sudden infant death syndrome (SIDS). Researchers will analyze the complete DNA of 650 infants who died from SIDS and both of their parents. By comparing these family trios, they hope to identify new genes or mutations linked to the condition. The goal is to better understand why SIDS happens and potentially develop ways to identify at-risk infants in the future.

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Contacts and locations

Study contacts

  • Contact

    Email: •••••@•••••

  • Contact

    Phone: •••-•••-•••• Email: •••••@•••••

Locations

  • AP-HM

    NOT_YET_RECRUITING

    Marseille, France

    Contact

  • APHP - Hôpital Antoine Béclère

    RECRUITING

    Clamart, France

    Contact

  • APHP - Hôpital Jean Verdier

    RECRUITING

    Bondy, France

    Contact

  • CHRU Nancy

    RECRUITING

    Nancy, France

    Contact

  • CHU Amiens

    RECRUITING

    Amiens, France

    Contact

  • CHU Angers

    RECRUITING

    Angers, France

    Contact

  • CHU Besançon

    RECRUITING

    Besançon, France

    Contact

  • CHU Brest

    RECRUITING

    Brest, France

    Contact

  • CHU Grenoble

    RECRUITING

    Grenoble, France

    Contact

  • CHU Montpellier

    RECRUITING

    Montpellier, France

    Contact

  • CHU Rouen

    RECRUITING

    Rouen, France

    Contact

  • CHU Saint Etienne

    RECRUITING

    Saint-Etienne, France

    Contact

  • CHU Toulouse

    RECRUITING

    Toulouse, France

    Contact

  • HCL

    RECRUITING

    Lyon, France

    Contact

  • Nantes University Hospital

    RECRUITING

    Nantes, Loire-Atlantique, 44093, France

    Contact Phone: •••-•••-•••• Email: •••••@•••••

Conditions

Explore the condition pages connected to this study.