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Blood Coagulation Disorders clinical trials

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NCT ID: NCT00056589 Completed - Clinical trials for Congenital Bleeding Disorder

Safety and Pharmacokinetics of Recombinant Factor XIII in Patients With Congenital Factor Xlll Deficiency

Start date: March 2003
Phase: Phase 1
Study type: Interventional

This trial was conducted in the United States of America (USA). The aim of this trial was to investigate safety and pharmacokinetics of escalating single doses of catridecacog (recombinant factor XIII, rFXIII) in patients with congenital factor XIII deficiency.

NCT ID: NCT00005481 Completed - Clinical trials for Cardiovascular Diseases

Epidemiology of Impaired Coagulant Balance in Diabetes

Start date: September 1996
Phase: N/A
Study type: Observational

To determine the nature, extent and molecular mechanisms responsible for impaired fibrinolysis in White, Black, Hispanic and American Indian populations with respect to the presence or absence of diabetes. The overall objective is to determine whether impairments of fibrinolysis underlie subclinical and clinical vascular disease in diabetes in specific populations with and without accelerated microvascular disease.

NCT ID: NCT00001927 Completed - Clinical trials for Cerebrovascular Accident

Study of Abnormal Blood Clotting in Children With Stroke

Start date: February 22, 1999
Phase: N/A
Study type: Observational

Effective treatment and prevention strategies for childhood stroke and porencephaly can only be developed once the causes are understood. There is increasing evidence that inherited and acquired coagulation abnormalities alone or in combination with environmental factors, predispose to arterial and venous thrombosis. Inherited abnormalities of factor V Leiden, prothrombin, protein C, protein S, and antithrombin III may account for many of these thromboses. At present there is little information on the existing distribution of these coagulation anomalies in children with thrombosis. Recent reports also suggest that these clotting abnormalities may be responsible for some instances of intracranial hemorrhage, porencephaly, cerebral palsy and fetal death. This study will measure the frequency of several coagulation factor abnormalities (factor V Leiden, prothrombin 20210A, protein C, protein S, antithrombin III, and antiphospholipid antibodies) in children with a history of porencephaly and stroke, and will compare these to the prevalence of these mutations in population controls and family members. We will also describe the exogenous conditions which in concert with these coagulation factors, may have led to the development of thrombosis in these children....

NCT ID: NCT00000582 Completed - Hemophilia A Clinical Trials

Cooperative Study of Factor VIII Inhibitors

Start date: July 1978
Phase: Phase 3
Study type: Interventional

To test the efficacy of prothrombin complex concentrates (Factor IX) in the treatment of hemophiliac patients who had inhibitors to Factor VIII.