Cord blood clues: scientists hunt for HHT treatment targets

NCT ID NCT05632484

First seen Nov 01, 2025 · Last updated May 14, 2026 · Updated 30 times

Summary

This study looked at cells from the umbilical cords of 16 newborns who had a parent with hereditary hemorrhagic telangiectasia (HHT), a rare disorder that causes abnormal blood vessels and bleeding. Researchers grew these cells in the lab to compare their genes with cells from healthy babies. The goal was to find new targets for future treatments. This was a basic science study, not a treatment trial, so there was no direct benefit to participants.

Disclaimer Read more

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.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for HEREDITARY HAEMORRHAGIC TELANGIECTASIA are added.

Our safety recommendation!

By submitting, you agree to our Terms of use

Contacts and locations

Locations

  • Hôpital Estaing

    Clermont-Ferrand, 63100, France

  • Hôpital Femme-mère-Enfant

    Bron, 69677, France

  • Hôpital St Eloi

    Montpellier, 34295, France

Conditions

Explore the condition pages connected to this study.