Italian researchers launch Largest-Ever study on rare genetic condition in children

NCT ID NCT06723938

First seen Mar 21, 2026 · Last updated May 14, 2026 · Updated 7 times

Summary

This study looks at 520 children and teens with a rare condition called 46, XY DSD, where a person's chromosomes (XY) don't match their physical sex development. Researchers will collect genetic and physical information to better understand the condition. The goal is to learn more, not to test a new treatment.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Study contacts

  • Contact

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

Locations

  • Azienda Ospedaliero Universitaria Pisana

    NOT_YET_RECRUITING

    Pisa, Pisa, 56126, Italy

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

    Contact

  • IRCCS Azienda Ospedaliero-Universitaria di Bologna

    RECRUITING

    Bologna, Bologna, 40138, Italy

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

    Contact

  • IRCCS Ospedale San Raffaele

    NOT_YET_RECRUITING

    Milan, Milano, 20132, Italy

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

    Contact

  • Ospedale Pediatrico Bambino Gesù

    NOT_YET_RECRUITING

    Roma, Roma, 00165, Italy

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

    Contact

Conditions

Explore the condition pages connected to this study.