5,000 hearts, one quest: scientists hunt for hidden genes behind birth defects

NCT ID NCT01192048

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study aims to find the genetic causes of congenital heart disease, the most common birth defect. Researchers will collect blood samples from 5,000 people with the condition and their family members. By analyzing their DNA, they hope to discover new genes that contribute to heart defects, which could lead to better diagnosis and future treatments.

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

What this could lead to

If successful, this could help identify new genes linked to congenital heart disease, improving diagnosis and future treatment targets.

What could go wrong

This is an observational study, not a treatment trial. It may not directly benefit participants, and finding genetic causes does not guarantee new therapies.

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.

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Conditions

The condition(s) this trial relates to.

Congenital Abnormalities congenital heart disease

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Study contacts

  • Contact

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

Locations

  • Nationwide Children's Hospital

    RECRUITING

    Columbus, Ohio, 43205, United States

    Contact