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Thrombocytopenia clinical trials

View clinical trials related to Thrombocytopenia.

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NCT ID: NCT01178333 Completed - Clinical trials for Heparin Induced Thrombocytopenia

Heparin-Induced Thrombocytopenia - Retrospective Analysis of Data on Incidence and Outcomes Study

HIT-RADIO
Start date: June 2010
Phase: N/A
Study type: Observational

HIT-RADIO is a study of patients who had a positive heparin PF-4 antibody test between 1/21/2008 and 9/25/2008 at selected hospitals. The study will collect and analyse information that is already in the patients' medical records. Information about laboratory values (such as platelet counts), treatments (such as medications), and outcomes (such as blood clots, amputation, and death) will be included.

NCT ID: NCT01165996 Completed - Clinical trials for Myelodysplastic Syndromes

Differentiation Therapy With Decitabine in Treating Patients With Myelodysplastic Syndrome

Start date: July 2010
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Decitabine may help myelodysplastic cells become more like normal stem cells. PURPOSE: This clinical trial studies differentiation therapy with decitabine in treating patients with myelodysplastic syndrome.

NCT ID: NCT01163110 Completed - Cancer Clinical Trials

Study to Investigate the Therapeutic Role of RNA Fragments in Platelet Production During Chemotherapy

Start date: March 2004
Phase: Phase 1
Study type: Interventional

The purpose of this study is to measure the therapeutic potential of Escherichia coli (E. coli) and yeast ribosomal Ribonucleic acid (RNA) fragments to maintain the production of platelets in patients undergoing cytotoxic therapy for cancer.

NCT ID: NCT01162941 Recruiting - Thrombocytopenia Clinical Trials

Efficacy of Helicobacter Pylori Eradication, Anti-D and Danazol Combination in Steroid Dependant or Refractory Immune Thrombocytopenia (ITP)

Start date: February 2010
Phase: Phase 2
Study type: Interventional

Proportion who would avoid splenectomy at 6 months of follow up

NCT ID: NCT01153919 Terminated - Thrombocytopenia Clinical Trials

Romiplostim in Treating Hepatitis C-Infected Patients With Thrombocytopenia

Start date: June 30, 2010
Phase: Phase 2
Study type: Interventional

RATIONALE: Romiplostim may cause the body to make platelets. PURPOSE: This randomized phase II trial is studying how well romiplostim works in treating hepatitis C-infected patients with thrombocytopenia.

NCT ID: NCT01147809 Completed - Thrombocytopaenia Clinical Trials

Safety and Efficacy Study for Solid Tumor Patients Treated With Eltrombopag

Start date: June 2010
Phase: Phase 2
Study type: Interventional

The present study is a randomized, blinded, placebo-controlled, two-Phase, sequential cohort, dose finding study to assess the safety and efficacy of eltrombopag in patients with solid tumors receiving gemcitabine monotherapy or the combination of gemcitabine plus carboplatin or cisplatin. Phase I of the study will examine safety and tolerability of various doses of eltrombopag to identify a dose and schedule of eltrombopag. Phase II will confirm that the chosen dose and schedule of eltrombopag from Phase I can deliver clinically meaningful benefit(s) to thrombocytopenic patients by improving platelet numbers.

NCT ID: NCT01143038 Completed - Clinical trials for Idiopathic Thrombocytopenic Purpura

Interventional Study in Adults With Immune Thrombocytopenia Purpura (ITP) Receiving Romiplostim

Start date: November 30, 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to describe the number of months with a platelet response over a 12 month treatment period and to describe ITP remission rates in adults with ITP receiving romiplostim.

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: NCT01129024 Terminated - Clinical trials for Immune Thrombocytopenia

An Open-label Safety Study of Lusutrombopag (S-888711) in Adults With Chronic Immune Thrombocytopenia (ITP)

Start date: April 29, 2010
Phase: Phase 2
Study type: Interventional

The primary objective of this study was to assess the long-term safety of lusutrombopag in the treatment of adults with relapsed persistent or chronic ITP with or without prior splenectomy.

NCT ID: NCT01102790 Recruiting - Thrombosis Clinical Trials

Generation of Heparin-induced Thrombocytopenia (HIT)-Antibodies Without Prior Heparin Exposure

Start date: April 2010
Phase: N/A
Study type: Observational

The purpose of this study is to determine the HIT-antibody generation without prior heparin-exposure in patients undergoing orthopedic surgery.