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Explore conditions, clinical trials, and the organisations running them.

Hemorrhagic disease

Spontaneous or near spontaneous bleeding caused by a defect in clotting mechanisms (blood coagulation disorders) or another abnormality causing a structural flaw in the blood vessels (hemostatic disorders).

108 trials tagged with this condition →

Hemophilia A 178 trials Sub-types →
Purpura 4 trials · 117 incl. sub-types Sub-types →
Hemophilia B 84 trials · 91 incl. sub-types Sub-types →
Vascular hemostatic disease 62 trials · 63 incl. sub-types Sub-types →
Hereditary von Willebrand disease 18 trials · 29 incl. sub-types Sub-types →
Inherited bleeding disorder, platelet-type 6 trials · 26 incl. sub-types Sub-types →
Acquired hemophilia 2 trials · 7 incl. sub-types Sub-types →
Factor VII deficiency 6 trials Sub-types →
Congenital fibrinogen deficiency 2 trials · 6 incl. sub-types Sub-types →
Fetal and neonatal alloimmune thrombocytopenia 4 trials Sub-types →
Congenital vitamin K-dependent coagulation factors deficiency 0 trials · 4 incl. sub-types Sub-types →
Acquired von willebrand syndrome 3 trials
Factor X deficiency 2 trials Sub-types →
Congenital factor XII deficiency 1 trial
Congenital plasminogen activator inhibitor type 1 deficiency 1 trial
East Texas bleeding disorder 0 trials
Alpha-2-plasmin inhibitor deficiency 0 trials
Combined deficiency of factor V and factor VIII 0 trials Sub-types →
Congenital factor V deficiency 0 trials
Congenital factor XI deficiency 0 trials
Congenital factor XIII deficiency 0 trials Sub-types →
Congenital high-molecular-weight kininogen deficiency 0 trials
Hemophilia B leyden 0 trials
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation 0 trials
Inherited prekallikrein deficiency 0 trials
Multiple sclerosis-ichthyosis-factor VIII deficiency syndrome 0 trials
Prothrombin deficiency 0 trials Sub-types →
Thrombomodulin-related bleeding disorder 0 trials