Familial hypofibrinogenemia

MONDO:0015096

Familial hypofibrinogenemia is a coagulation disorder characterized by mild bleeding symptoms following trauma or surgery due to a reduced plasma fibrinogen concentration.

Also known as: hypofibrinogenemia, familial

13 clinical trials for this condition and its sub-types, 3 tagged with Familial hypofibrinogenemia itself.

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Where it sits in the disease tree

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Part of

↑ Congenital afibrinogenemia (5)

Including sub-types (13) Tagged with Familial hypofibrinogenemia (3)

Trials to join now! 7 Not yet recruiting 3 Not yet finished but already full! 1 Completed 2

AI takes on blood clotting: can ChatGPT guide surgeons on bleeding?

Knowledge-focused Cancelled

This study evaluates whether artificial intelligence models can accurately interpret ROTEM blood clotting tests and recommend treatments for coagulopathy. Researchers will compare AI decisions to those of a panel of clinical experts using data from adults undergoing elective card…

Sponsor: Ondokuz Mayıs University • Aim: Knowledge-focused

Last updated Jul 04, 2026 00:00 UTC

Familial hypofibrinogenemia

Where it sits in the disease tree

AI takes on blood clotting: can ChatGPT guide surgeons on bleeding?