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Double check: new study aims to catch hidden thyroid issues in preemies

NCT ID NCT07425028

First seen Feb 28, 2026 · Last updated May 25, 2026 · Updated 4 times

Summary

This study will test a new, two-step screening method for congenital hypothyroidism (a thyroid hormone deficiency) in premature babies born before 32 weeks. Currently, France uses a single test, but European guidelines recommend repeating the test within the first month. Researchers will screen 1,600 newborns to see if the double test finds more cases, helping ensure these babies get the treatment they need early on.

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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

  • Chu de Lille

    Lille, France

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

Conditions

Explore the condition pages connected to this study.