Rare bleeding disorder study seeks to unlock antibody mystery
NCT ID NCT04595617
First seen Jun 27, 2026 · Last updated Jun 27, 2026
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.
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.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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CHU Bordeaux - Hôpital Haut-Lévêque
Bordeaux, France
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CHU Bordeaux - Hôpital Pellegrin
Bordeaux, France
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CHU Nîmes
Nîmes, France
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CHU Strasbourg
Strasbourg, France
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CHU Toulouse
Toulouse, France
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Hôpital Bicêtre, APHP
Le Kremlin-Bicêtre, France
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Hôpital la Timone, APHM
Marseille, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Massive blood disorder registry aims to transform care
- New blood test could unmask hidden bleeding disorders
- New antibody aims to stop bleeding episodes in rare clotting disorder
- Scientists dig into genetic roots of rare bleeding disorders