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Rare bleeding disorder study seeks to unlock antibody mystery

NCT ID NCT04595617

First seen May 24, 2026 · Last updated Jun 23, 2026 · Updated 6 times

Summary

This study looked at 28 people with Glanzmann thrombasthenia, a rare bleeding disorder, to understand why some develop harmful antibodies after blood transfusions or pregnancy. Researchers checked for antibodies every six months and after each transfusion over 18 months. The goal was to link genetic, treatment, and lifestyle factors to antibody formation.

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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

Locations

  • CHU Bordeaux - Hôpital Haut-Lévêque

    Bordeaux, France

  • CHU Bordeaux - Hôpital Pellegrin

    Bordeaux, France

  • CHU Nîmes

    Nîmes, France

  • CHU Strasbourg

    Strasbourg, France

  • CHU Toulouse

    Toulouse, France

  • Hôpital Bicêtre, APHP

    Le Kremlin-Bicêtre, France

  • Hôpital la Timone, APHM

    Marseille, France

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 study could help doctors predict and reduce the risk of antibody formation in Glanzmann thrombasthenia patients, improving transfusion safety.

What could go wrong

This is a small observational study (28 people) that only measures antibodies, not a treatment. It may not lead to direct changes in care.

Conditions

The condition(s) this trial relates to.

Glanzmann thrombasthenia 1

As listed by the trial registrant

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