Cure My Disease

Don't miss your cure!

Log in / Sign up

Fibrinolytic defect

MONDO:0007605

Also known as: fibrinolytic defect

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

Follow this condition to get notified about new trials

Broader categories

Disease (717) Hereditary disease (188) Human disease (15) Disease of genetic or genomic mechanism (2) Disease by etiologic mechanism (0)

Trials to join now! 1 Completed 2

Could your genes raise your risk of a mystery stroke?

Knowledge-focused Recruiting now

This study is looking at whether certain gene changes (variants) in a protein called annexin A2 are linked to strokes that happen for no clear reason, especially in younger adults. Researchers will compare blood samples from 240 people who have had a stroke with no known cause. T…

Sponsor: Centre Hospitalier Universitaire, Amiens • Aim: Knowledge-focused

Last updated Jun 27, 2026 08:11 UTC