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Thrombocytopenia clinical trials

View clinical trials related to Thrombocytopenia.

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NCT ID: NCT01226524 Terminated - Clinical trials for Childhood Chronic Immune Thrombocytopenia

The Role of Traditional Chinese Medicine in the Treatment of Chronic Childhood Immune Thrombocytopenia (ITP)

Start date: February 2011
Phase: Phase 2/Phase 3
Study type: Interventional

Immune thrombocytopenia (ITP) is an autoimmune disorder manifested as isolated low platelet count which results in a tendency for bleeding. Around 10% of childhood ITP does not reach resolution within 1 year thus becoming chronic ITP. Therapeutic modalities at present are aimed to achieve symptomatic relief, do not change the natural course of the disorder and are associated with potential side effects and increase cost. Thus, identifying a new therapy that would decrease the bleeding symptoms, without causing significant adverse effects, could be very beneficial. Preliminary reports demonstrate a beneficial role for Traditional Chinese medicine (TCM) in the treatment of ITP. Working hypothesis and aims: The use of TCM will improve the status of children with chronic ITP and thus will reduce the need to use conventional medications. The investigators aim to study whether in children with chronic ITP, supplementation with TCM, improves the bleeding symptoms and ITP-related quality of life (QOL) compared to the period prior to the intervention? Methods: The study includes three periods: 1st observation period (1 month), TMC period (3 months) and 2nd observation period (2 months). During all study periods the following data will be collected: bleeding symptoms, bleeding score, platelet count, need for conventional therapy, side effects of therapy and ITP-related QOL.

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: 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: NCT01054443 Terminated - Clinical trials for Immune Thrombocytopenia (ITP)

A Study to Investigate the Efficacy and Safety of Lusutrombopag (S-888711) Tablets Administered to Adults With Immune Thrombocytopenia (ITP)

Start date: March 18, 2010
Phase: Phase 2
Study type: Interventional

The primary objective of this study was to assess the efficacy of 3 dose levels of lusutrombopag (0.5 mg, 0.75 mg, and 1.0 mg) and placebo on platelet count.

NCT ID: NCT00931762 Terminated - Clinical trials for Primary Myelofibrosis

A Study to Evaluate Safety and Efficacy of Panobinostat in Participants With Primary Myelofibrosis

Start date: August 31, 2009
Phase: Phase 2
Study type: Interventional

This study assessed the safety and efficacy of Panobinostat as a single agent in the treatment of Primary Myelofibrosis, Post-Polycythemia Vera and Post-Essential Thrombocythemia. There were two cohorts - participants with JAK2 mutation and participants without JAK2 mutation.

NCT ID: NCT00926354 Terminated - Clinical trials for Chemotherapy Induced Thrombocytopenia

Application of AS101 for the Treatment of Thrombocytopenia in Solid Tumor Patients

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

Chemotherapy Induced Thrombocytopenia is a common side-effect of bone marrow suppression as a result of a chemotherapy treatment. AS101 is a tellurium based small compound with immunomodulating characteristics which attributed to the direct inhibition of the anti-inflammatory cytokine IL-10. AS101 was previously shown to induce a significant reduction in thrombocytopenia that accompany cancer therapy with no major toxicity . This phase II randomized open study will evaluate the efficacy of AS101 for the treatment of chemotherapy induced thrombocytopenia in patients with various solid tumors.

NCT ID: NCT00909363 Terminated - Bleeding Clinical Trials

Thrombocytopenia and Bleeding in Wiskott-Aldrich Syndrome (WAS) Patients

WAS
Start date: June 2009
Phase: Phase 2
Study type: Interventional

The purpose of this project is to describe the pathophysiology of thrombocytopenia and bleeding in patients with Wiskott-Aldrich Syndrome (WAS) and determine the response to thrombopoietic agents in vitro and in vivo.

NCT ID: NCT00886743 Terminated - Clinical trials for Severe Thrombocytopenia

Study Evaluating The Effects Of Oprelvekin On Cardiac Repolarization In Subjects With Chemotherapy Induced Thrombocytopenia

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

This is an open-label study in which oprelvekin will be administered for the prevention of severe low blood platelet cell counts (cells in your blood that keep bleeding and clotting stable) in adults with cancer who are taking chemotherapy (anti-cancer drug) that has a side effect of blocking your bone marrow from making platelet cells. The purpose of this study is to learn more about the effects of the recommended dose of oprelvekin on the heart's electrical cycle.

NCT ID: NCT00882414 Terminated - Clinical trials for Iron-Deficiency Anemia

Ferinject® in Patient With Thrombocytosis Secondary to Inflammatory Bowel Disease (IBD)

Start date: December 2006
Phase: Phase 2
Study type: Interventional

The aim of this study is to show the benefits for patients, with a high platelet count, iron deficiency and IBD, receiving intravenous iron therapy.

NCT ID: NCT00798525 Terminated - Clinical trials for Heparin Induced Thrombocytopenia (HIT)

Argatroban Versus Lepirudin in Critically Ill Patients

ALiCia
Start date: January 2009
Phase: Phase 4
Study type: Interventional

The purpose of this study is to test the hypotheses that argatroban significantly increases efficacy and safety of renal replacement therapy measured as life time of haemodialysis filters as compared to lepirudin