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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

47 clinical trials for this condition and its sub-types.

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Broader categories

Disease (618) Hematologic disorder (160) Hemorrhagic disease (100) Blood coagulation disease (51) Human disease (14) Coagulation protein disease (12) Congenital afibrinogenemia (4) Congenital fibrinogen deficiency (2) Familial dysfibrinogenemia (2) Disease by body system or component (0)

Trials to join now! 22 Not yet recruiting 5 Not yet finished but already full! 5 Completed 14 Terminated 1

Can extra care after transplant help older patients live better?

Disease control Terminated

This study tested two extra care programs—supportive palliative care and clinical management of other health issues—for older or frail patients who had a donor stem cell transplant. The goal was to see if these programs could improve quality of life and survival compared to stand…

Phase: PHASE2, PHASE3 • Sponsor: Fred Hutchinson Cancer Center • Aim: Disease control

Last updated Jun 27, 2026 08:10 UTC