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Thrombocytopenia clinical trials

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NCT ID: NCT02717039 Recruiting - Clinical trials for Heparin-induced Thrombocytopenia

Pharmacogenomics of Heparin-Induced Thrombocytopenia

PHIT
Start date: March 2016
Phase:
Study type: Observational

The purpose of this research is to identify genomic markers that can predict heparin-induced thrombocytopenia (HIT), which is a very serious side effect to heparin. Heparin is commonly used to prevent blood clots and the investigators may be able to identify genomic markers which can be used to prevent heparin use in people who will get HIT.

NCT ID: NCT02707497 Recruiting - Sepsis Clinical Trials

The Effect of REcombinant Human Thrombopoietin (rhTPO) on Sepsis Patients With aCUte Severe thrombocytopEnia

RESCUE
Start date: April 1, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to determine whether recombinant human thrombopoietin(rhTPO) can rapidly increase the platelets counts, shorten the time of the platelet returned to normal, reduce platelet transfusion and bleeding events, prompt recovery of organ function, decrease the length of ICU stay, and eventually reduce the 28-day mortality in sepsis patients with severe thrombocytopenia.

NCT ID: NCT02627417 Recruiting - Dapsone Clinical Trials

Efficacy and Safety of DAPSone as a Second-line Option in Adult Immune Thrombocytopenia

DAPS-ITP
Start date: December 2015
Phase: Phase 3
Study type: Interventional

Due to its expected efficacy based on the retrospective data available in ITP, its relatively good safety profile and its very low cost , dapsone could be a good steroid-sparing second-line option for adults with ITP. This study is a phase III prospective multicenter randomized open trial comparing two treatment strategies: - Arm A (experimental arm): prednisone at 1 mg/kg for 3 weeks + dapsone at 100 mg per day up to week 52 if an initial response is achieved. - Arm B (control arm): prednisone alone at 1 mg/kg for 3 weeks followed by monitoring and "standard of care" The aim of the study is to demonstrate the efficacy of dapsone based on the overall response rate (including response and complete response) as a second-line treatment for adults with newly-diagnosed persistent or chronic (modified by amendment 08/11/2016) ITP not achieving a durable response with corticosteroids. The primary endpoint will be the overall response-rate (response or complete response according to standard definitions) in both arms at week 52 (1 year). The secondary endpoints are the following : - To assess the safety of dapsone over the study period and especially the incidence of cutaneous reactions. - To analyze the overall response rate (platelet count > 30 x 109/L with at least a doubling of the pre-treatment count in the absence of any other ITP treatment) in both treatment arms at week 24. - To compare the rate of complete response and failure in both arms at 24 and 52 weeks. - To compare time to treatment failure (TTF) in both arms - To investigate the mechanisms of action of dapsone in ITP in a subgroup of patients (ancillary study)

NCT ID: NCT02298075 Recruiting - Clinical trials for Immune Thrombocytopenia

Response Rate and Duration After Discontinuation Thrombopoietin Receptor Agonists Primary Immune Thrombocytopenia

Start date: April 2016
Phase:
Study type: Observational

The primary objective of the study is the evaluation of sustained response rate after discontinuation of treatment with TPO-RAs, Eltrombopag and Romiplostim, in persistent or chronic pITP patients who failed one or more therapy lines, splenectomy included.

NCT ID: NCT02270801 Recruiting - Pregnancy Clinical Trials

Recombinant Human Thrombopoietin (rhTPO) in Management of Immune Thrombocytopenia (ITP) in Pregnancy

Start date: October 2014
Phase: Phase 3
Study type: Interventional

This clinical trial is undertaking by Qilu Hospital of Shandong University, aims at evaluating efficacy and safety of rhTPO in management of ITP in pregnancy.

NCT ID: NCT02244658 Recruiting - Thrombocytopenia Clinical Trials

Recombinant Human Thrombopoietin (rhTPO) in Management of Chemotherapy-induced Thrombocytopenia in Acute Myelocytic Leukemia

Start date: September 2014
Phase: Phase 3
Study type: Interventional

Chemotherapy-related myelosuppression usually occurs in AML patients, which induces severe thrombocytopenia and haemorrhage, a leading cause of death. This clinical trial aims at evaluating efficacy and safety of rhTPO in management of chemotherapy-induced thrombocytopenia in acute myelocytic leukemia.

NCT ID: NCT02241031 Recruiting - Thrombocytopenia Clinical Trials

Megakaryocytic Progenitor Cells for Prophylaxis and Treatment of Thrombocytopenia

Start date: September 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy of ex vivo generated megakaryocytic progenitor cells (MPs) in prophylaxis and treatment of thrombocytopenia caused by chemotherapy in patients with acute leukemia (AL).

NCT ID: NCT02094248 Recruiting - Sepsis Clinical Trials

rhTPO in Critical Patients With Thrombocytopenia

Start date: March 2014
Phase: Phase 2/Phase 3
Study type: Interventional

The primary objectives of this study are to assess the impact of rhTPO on mortality among severe sepsis patients with thrombocytopenia, as well as changes of platelet counts and platelet transfusion rates.

NCT ID: NCT01970189 Recruiting - Thrombocytopenia Clinical Trials

The International ITP Registry

Start date: January 2011
Phase: N/A
Study type: Observational [Patient Registry]

Primary immune thrombocytopenia (ITP) is an uncommon disease characterised by a low platelet count, which may cause the patient to have a higher risk or increased duration of bleeding. Individual hospitals only encounter a small number of ITP patients each year which makes it difficult to study this disease. By creating this disease registry, we will be able to build a more complete picture of ITP, including treatment practices, through collecting information about the condition from patients across several hospitals in several countries. Research of this kind will help future patients by providing doctors with information about ITP, and about how patients have been treated.

NCT ID: NCT01805648 Recruiting - Thrombocytopenia Clinical Trials

Efficacy and Safety Study of Maintenance Treatment With rhTPO in Thrombocytopenic Subjects With ITP

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

The purpose of this study is to evaluate the efficacy and safety of rhTPO in the maintenance treatment of ITP, to explore the appropriate dosing interval of the maintenance treatment of rhTPO .