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Hemolysis clinical trials

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NCT ID: NCT02976610 Completed - Hemolysis Clinical Trials

Clinical Study of a Novel Hemolysis Point of Care Test at an Emergency Department.

Start date: December 1, 2016
Phase: N/A
Study type: Interventional

This study aims to investigate the outcome of hemolysis frequency when a hemolysis point of care test is introduced in an emergency department.

NCT ID: NCT02949128 Completed - Clinical trials for Atypical Hemolytic Uremic Syndrome (aHUS)

Study of ALXN1210 in Complement Inhibitor Treatment-Naïve Adult and Adolescent Participants With Atypical Hemolytic Uremic Syndrome (aHUS)

Start date: January 11, 2017
Phase: Phase 3
Study type: Interventional

The purpose of the study is to assess the safety and efficacy of ravulizumab to control disease activity in adolescent and adult participants with aHUS who had not previously used a complement inhibitor.

NCT ID: NCT02924792 Completed - Hemorrhagic Shock Clinical Trials

Sternal Intraosseous Transfusion of Autologous Whole Blood: A Comparison of Flow Rates and Degree of Hemolysis

Start date: November 2016
Phase: N/A
Study type: Observational

In this study the impact of two CE marked and FDA approved sternal needles in comparison to intravenous access on the flow-rate of autologous reinfusion of whole blood and the possible hemolysis of red cells post-transfusion in a population of healthy military officers is investigated.

NCT ID: NCT02904863 Completed - Clinical trials for Hemolytic Uremic Syndrome

Study of 'Vascular Competence' Profile and Endothelial Activation in the Hemolytic Uremic Syndrome in Children and Adults

SHU
Start date: February 11, 2013
Phase: N/A
Study type: Interventional

The Hemolytic Uremic Syndrome (HUS) is a rare thrombotic microangiopathy (TMA), affecting both children and adults. HUS is characterized by the abnormal occurrence of diffuse thrombosis in the microcirculation resulting in the occurrence of ischemic events affecting especially the kidneys and is associated with hemolytic anemia. One of the major problems encountered in the management of HUS is the absence of reliable marker of treatment response or relapse; conventional hematological markers being too insensitive to judge therapeutic efficacy or identify early relapse. Data from the literature suggest that the endothelial cell is a major target of this syndrome. Our hypothesis is that an initial micro-endothelial activation plays a critical role in the initiation and / or relapse of the disease.The main objective of this study is to define a "vascular competence" profile in a population of patients with typical or atypical HUS; both in the acute phase and in remission of the disease.

NCT ID: NCT02877706 Recruiting - Clinical trials for Immune Thrombocytopenia

French Registry of Adult Patients With Immune Thrombocytopenia and Autoimmune Hemolytic Anemia

CARMEN
Start date: June 2013
Phase:
Study type: Observational [Patient Registry]

CARMEN is a national, real-world clinical registry of all adult patients with incident diagnosis of Immune thrombocytopenia (ITP) or Autoimmune Hemolytic anemia (AIHA) patients in France. It is aimed at describing ITP and AIHA clinical features, assessing the real-world risk-benefit ratio of treatments and adherence to guidelines for ITP and AIHA management.

NCT ID: NCT02828670 Recruiting - Clinical trials for Autoimmune Hemolytic Anemia

Role of T Follicular Helper Cells in Autoimmune Hemolytic Anemia (TFH in AIHA)

TFH and AIHA
Start date: June 7, 2016
Phase:
Study type: Observational

T follicular helper (TFH) cells represent a T cell subset dedicated to the activation of B cells. They have been involved in the pathogenesis of autoimmune diseases in humans such as lupus and Sjögren disease. We recently showed that TFH are implicated in the activation of autoreactive B lymphocytes during ITP. Autoimmune hemolytic anemia (AIHA) is an autoimmune disease due to antibodies targeting red blood cells. To date, the role of TFH in the pathogenesis of AIHA is not known. We hypothesize that AIHA is associated with an increase in the number and/or function of TFH, that could participate in the activation of autoreactive B lymphocytes.

NCT ID: NCT02711332 Completed - Hemolysis Clinical Trials

Investigating the Influence of Haemolysis on the Potassium Concentration After Capillary Blood Sampling

Start date: June 2015
Phase: N/A
Study type: Observational

This is an open, single-centre trial investigating the impact of haemolysis after capillary blood collection to the measured potassium concentration in Plasma healthy subjects. Each subject will have four capillary blood collections on different fingers. Two on the right and two on the left hand. Additionally as a reference a venous blood collection will be conducted.

NCT ID: NCT02689986 Completed - Clinical trials for Autoimmune Hemolytic Anemia

Bendamustine and Rituximab Combination Therapy for Cold Agglutinin Disease

CAD5
Start date: January 2013
Phase: Phase 2
Study type: Interventional

Prospective, non-randomized multicenter study on the safety and efficacy of combination therapy with bendamustine and rituximab for chronic cold agglutinin disease.

NCT ID: NCT02626663 Withdrawn - Clinical trials for Thrombotic Thrombocytopenic Purpura

The Role of Microparticles as a Biomarker

Start date: July 2016
Phase:
Study type: Observational

The investigators propose to characterize MPs in aHUS and TTP both at the onset and throughout treatment. The investigators believe that the number, size, and cell origin of MPs will differ between these two diseases. The hypothesis is that endothelial derived MPs will be higher in number and comprise a larger portion of the MP population in aHUS and that platelet MPs will comprise a larger number and greater proportion of MPs in TTP. The investigators believe that MP identity and number can be used to reliably differentiate between aHUS and TTP at disease onset.

NCT ID: NCT02614898 Terminated - Clinical trials for Atypical Hemolytic Uremic Syndrome

Evaluation of Potential Predictors of Disease Progression in Participants With Atypical Hemolytic Uremic Syndrome (aHUS) Including Genetics, Biomarkers, and Treatment

EVIDENCE
Start date: November 4, 2015
Phase:
Study type: Observational

This was a prospective, open-label study with no participant randomization. Treatment for aHUS was observational and at the discretion of the treating physician. The purpose of this study was to assess disease manifestations of complement-mediated thrombotic microangiopathy (TMA) and evaluate potential clinical predictors of disease manifestations and progression in participants with aHUS with or without eculizumab treatment in the clinical setting.