Scientists hunt for hidden genes behind common bleeding disorder
NCT ID NCT05116501
First seen Jun 08, 2026 · Last updated Jun 22, 2026 · Updated 4 times
Summary
This study looked at the DNA of 254 people to find genetic reasons for low von Willebrand factor, a mild bleeding condition. Researchers used whole-exome sequencing to check for changes in known and new genes. The goal was to better understand why some people have low levels of this clotting protein.
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This is a summary of
the original study
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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.
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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Genom att skicka in godkänner du våra Användarvillkor
Contacts and locations
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Genom att skicka in godkänner du våra Användarvillkor
Locations
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Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, A.B.Bonomi Hemophilia and Thrombosis Center
Milan, Lombardy, 20122, Italy
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 research could identify new genes that cause low von Willebrand factor, leading to better diagnosis and understanding of the condition.
What could go wrong
This is an observational study, not a treatment trial. It may not find clear genetic causes, and results may not change patient care directly.
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.