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Blood Platelet Disorders clinical trials

View clinical trials related to Blood Platelet Disorders.

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NCT ID: NCT01361620 Completed - Clinical trials for Platelet Dysfunction Due to Aspirin

Genotypic and Phenotypic Correlates of Resistance to Aspirin

ARSENAL
Start date: December 2007
Phase: N/A
Study type: Interventional

The study seeks to identify genomic markers associated with aspirin resistance.

NCT ID: NCT01133860 Completed - Clinical trials for Blood Platelet Disorders

Efficacy of Eltrombopag to Improve Thrombocytopenia of MYH9-related Disease

Start date: January 2009
Phase: Phase 2
Study type: Interventional

The term MYH9-related disease (MYH9RD) includes four genetic disorders: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome. All these disorders derive from mutation of a unique gene, named MYH9, and they have been recognized as different clinical presentations of a single illness that was named MYH9RD. All patients affected by MYH9RD present since birth with thrombocytopenia, which can result in a variable degree of bleeding diathesis; some of them subsequently develop additional clinical manifestations, such as renal damage, sensorineural hearing loss, and/or presenile cataracts. Eltrombopag is an oral thrombopoietin receptor agonist that stimulates proliferation and differentiation of megakaryocytes, the bone marrow cells that produce blood platelets. This drug is effective in increasing platelet count in healthy volunteers, as well as in patients affected by some acquired thrombocytopenias, such as idiopathic thrombocytopenic purpura and HCV related thrombocytopenia. The purpose of this study is to determine if eltrombopag, administered orally at the dose of 50 or 75 mg/daily for up to 6 weeks, is effective in increasing platelet count of patients affected by MYH9RD. Further aims of this study are to test if eltrombopag is effective in reducing bleeding tendency of MYH9RD patients; to evaluate safety and tolerability of eltrombopag in patients with MYH9RD; to evaluate in vitro function of platelets produced during therapy in patients responding to this drug.

NCT ID: NCT00168090 Completed - Clinical trials for Blood Coagulation Disorders

Study of Safety and Efficacy of Antihemophilic Factor/Von Willebrand Factor Complex in Surgical Subjects With Von Willebrand Disease (vWD)

Start date: October 2001
Phase: Phase 4
Study type: Interventional

The purpose of this study is to test the safety and effectiveness of Humate-P® to prevent bleeding in patients with von Willebrand Disease who are undergoing surgery.

NCT ID: NCT00115375 Completed - Clinical trials for Congenital Heart Defects

Platelet Aggregation Inhibition in Children on Clopidogrel (PICOLO)

Start date: January 2004
Phase: Phase 2
Study type: Interventional

PICOLO is a double blind placebo controlled phase II dose ranging, dose escalating study in patients of Blalock-Taussig age categories (neonates and infants/toddlers), to determine the dose providing inhibition of platelet aggregation similar to adults.

NCT ID: NCT00111215 Completed - Menorrhagia Clinical Trials

Treatment and Management of Women With Bleeding Disorders

Start date: January 2001
Phase: N/A
Study type: Interventional

The purpose of the study is to determine whether oral contraceptives, desmopressin acetate, and/or tranexamic acid are effective in the treatment of women with menorrhagia who are diagnosed with a bleeding disorder.