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Purpura clinical trials

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NCT ID: NCT02877212 Recruiting - Clinical trials for Immune Thrombocytopenic Purpura (ITP)

Association of FcγRIIIA Polymorphism and THPO Expression With Response to Eltrombopag in Refractory ITP Patients

Start date: July 2016
Phase: Phase 3
Study type: Interventional

Idiopathic thrombocytopenic purpura (ITP) is an autoimmune disease characterized by antibody-mediated platelet destruction. The complex pathogenesis of ITP with multiple challenges to immune system in terms of genetic predisposition, infection, responsiveness to immunosuppressive therapy (IST) and inhibition of platelet production has proven the diversity of constraints in diagnosing and treating ITP. Thrombopoietin receptor agonist (Eltrombopag) is specifically indicated for the treatment of thrombocytopenia in patients with chronic immune (idiopathic) thrombocytopenic purpura (ITP) who have had an insufficient response to corticosteroids, immunoglobulins, or splenectomy. This clinical trial aims to investigate the association of Fc gammaRIIIA gene (V158F) genetic predisposition with treatment outcome of Immune Thrombocytopenia (ITP) in refractory ITP patients and especially with Eltrombopag.

NCT ID: NCT02614846 Recruiting - Clinical trials for Chronic Idiopathic Thrombocytopenic Purpura

Safety and Efficacy Study of Hetrombopag Olamine in Chronic Idiopathic Thrombocytopenic Purpura (ITP) Patients

Start date: August 2015
Phase: Phase 1
Study type: Interventional

This study evaluates the safety and efficacy of 6 weeks dosing Hetrombopag Olamine in Chronic Idiopathic Thrombocytopenic Purpura Patients. All of the subjects in this study receive Hetrombopag.

NCT ID: NCT02593565 Recruiting - Vasculitis Clinical Trials

Vasculitis Pregnancy Registry

V-PREG
Start date: November 2015
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to learn about the experience of women with vasculitis who become pregnant. In particular, the study will consist of several online surveys to assess 1. each woman's vasculitis severity and pregnancy-related experiences, and 2. pregnancy outcomes.

NCT ID: NCT02540720 Recruiting - Clinical trials for Henoch-Schoenlein Purpura

The Research of Standard Diagnosis and Treatment for Severe HSP in Children

Start date: August 2015
Phase: Phase 2
Study type: Interventional

This study is performed to evaluate the efficacy and safety of various measures in the treatment of severe HSP in children.

NCT ID: NCT02532790 Recruiting - Clinical trials for Henoch-Schoenlein Purpura Nephritis

The Research of Standard Diagnosis and Treatment for HSPN With Mild Proteinuria in Children

Start date: August 2015
Phase: Phase 2
Study type: Interventional

This study is performed to evaluate the efficacy and safety of various measures in the treatment of HSPN with mild proteinuria in children.

NCT ID: NCT02532777 Recruiting - Clinical trials for Henoch-Schoenlein Purpura Nephritis

The Research of Standard Diagnosis and Treatment for HSPN in Children

Start date: August 2015
Phase: Phase 2
Study type: Interventional

This study is performed to evaluate the efficacy and safety of various measures in the treatment of HSPN in children.

NCT ID: NCT02403440 Recruiting - Clinical trials for Purpura, Thrombocytopenic, Idiopathic

A Study of Hetrombopag Olamine in Chronic Idiopathic Thrombocytopenic Purpura (ITP) Patients

Start date: April 2014
Phase: Phase 1
Study type: Interventional

The purpose of this study is to obtain information on efficacy, safety and Pharmacokinetics (PK)/Pharmacodynamics (PD) of Hetrombopag over 14 days in Chinese patients with chronic ITP.

NCT ID: NCT01648556 Recruiting - Clinical trials for Purpura Thrombopenic

Research of Predictive Factors to Immune Thrombopenic Purpura

PREDI-PTI
Start date: September 2012
Phase: N/A
Study type: Interventional

It is about a multicentric study prospective of more than patients' 60 years with a thrombopenia isolated of less than 100 G/L blood platelet without cause found to estimate so certain examinations realized in the diagnosis (medullary cytogenetics, dosage of the TPO, the Anti-platelet antibodies, isotopic lifetime of platelet) are in favour of the diagnosis of PTI.

NCT ID: NCT01610830 Recruiting - Clinical trials for Purpura, Schoenlein-Henoch

Identification of Biomarkers Predictive of Worse Prognosis in Henoch Schonlein Purpura

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

Henoch Schonlein Purpura (HSP), vasculitis of small vessels with deposits of IgA, is considered by many authors as the systemic form of Berger's disease (IgA-N). IgA-N is characterized by IgA1 deposits in mesangial areas associated with mesangial proliferation. These two diseases remain the leading cause of ESRD by primitive glomerulopathy in Western countries. In recent years, considerable progress has been made in understanding the pathophysiological mechanisms of IgA-N. However, only a high rate of proteinuria at one year or the presence of severe glomerular inflammation on renal biopsy remain predictors of long term renal function. Moreover, the high variability of HSP clinical expression, from few purpura skin lesions that evolve favourably spontaneously, to rapidly progressive renal failure, remains so far unexplained but suggests the existence of individual genetic susceptibility. In the first part of the study, we will study key factors based on physiopathological data obtained by our laboratory as well as by other groups. The second part of the study concerns genetic factors. Although the candidate genes that may confer a particular susceptibility to the disease, to progress to ESRD or respond to treatment are many, the genes involved in inflammation or controlling renin-angiotensin system are of particular interest. We will apply these results by studying patients with HSP showing three distinct phenotypes (HSP with isolated cutaneous purpura or associated with minimal or severe renal disease) at diagnosis and after clinical remission. The purpose of this study is to assess whether the phenotype at diagnosis is associated with the physiological markers and if one of them predicts a pejorative evolution of renal disease at 1 year. Meanwhile, study of polymorphism of selected genes of interest could allow identification of patients with specific genetic susceptibility or with bad prognosis factors who would be thus eligible for specific treatment.

NCT ID: NCT01485367 Recruiting - Senile Purpura Clinical Trials

A Pilot Study to Evaluate The Efficacy of Adapalene 0.3% for Use in the Prevention and Treatment of Senile Purpura

Start date: December 2011
Phase: Phase 2
Study type: Interventional

This is an open label 6 month pilot study for male and female participants over the age of 52 that desire treatment and prevention of senile purpura of the forearms. This study will be evaluating the effects of Adapalene 0.3% for the use in the treatment and prevention of senile purpura.