New blood test could replace risky amniocentesis for genetic disorders

NCT ID NCT03743948

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

Summary

This study tested a new blood test that looks for fetal cells in the mother's blood to diagnose genetic diseases in the baby. It aimed to replace invasive tests like amniocentesis, which carry a small risk of miscarriage. The trial enrolled 18 pregnant women but was terminated early, so we don't yet know if the test works well enough.

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 offer a safer, non-invasive way to diagnose genetic disorders in unborn babies, reducing the need for risky procedures like amniocentesis.

What could go wrong

The trial was terminated early with only 18 participants, so results are limited. The test may fail due to low fetal cell counts or technical issues, and it is not yet proven reliable.

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.

hereditary disease

As listed by the trial registrant

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

Contacts and locations

Locations

  • INSERM-Hospital,

    Montpellier, Herault, 34295, France