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Hemolysis clinical trials

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NCT ID: NCT02205541 Completed - Clinical trials for Hemolytic Uremic Syndrome of Childhood

Eculizumab in Shiga-toxin Related Hemolytic and Uremic Syndrome Pediatric Patients - ECULISHU

ECULISHU
Start date: June 2015
Phase: Phase 3
Study type: Interventional

The investigators aim to perform the first controlled randomized prospective study using ECZ in pediatric STEC-HUS. This is of great interest as there is still no efficient specific therapy in that potentially devastating disease. Furthermore, published data concerning the use of ECZ in STEC-HUS are controversial, reflecting statistical bias in retrospective or uncontrolled studies, thus emphasizing the need for prospective studies.

NCT ID: NCT02158195 Completed - Clinical trials for Autoimmune Hemolytic Anemia

Immunopathology of Autoimmune Hemolytic Anemia

IAHAI
Start date: July 3, 2013
Phase:
Study type: Observational

Autoimmune hemolytic anemia (AIHA) is an auto-immune disease mediated by specific antibodies targeting red blood cells. Its pathogenesis is not completely understood, and the role of T cells have been rarely studied. The aim of this study is to compare the frequency of circulating T cells, T cell polarization and functions, notably regulatory T cells, during warm AIHA by comparison to healthy controls. The role of treatments, such as steroids, will also be determined in patients with warm AIHA.

NCT ID: NCT02111590 Completed - Clinical trials for Chronic Inflammatory Demyelinating Polyneuropathy

Immunoglobulin Dosage and Administration Form in CIDP and MMN

Start date: January 2014
Phase: N/A
Study type: Observational

The aim of this study is to evaluate development of hemolysis and the variation in isokinetic muscle strength in two groups of patients with chronic inflammatory demyelinating polyneuropathy (CIDP) or multifocal motor neuropathy (MMN) 1. Patients shifted from 3- or 6-weekly treatment with intravenous immunoglobulin (IVIG) to weekly treatment with subcutanoeus immunoglobulin (SCIG) 2. Patients shifted from SCIG treatment with Subcuvia® or Hizentra® to Gammanorm®. Hypotheses - During treatment with IVIG blood hemoglobin will fluctuate with a decline due to infusion, whereas it will remain stable during SCIG treatment without fluctuation - Isokinetic muscle strength in affected muscle groups is more stable during treatment with SCIG than with IVIG - Blood hemoglobin and changes in muscle strength is comparable during Subcuvia® or Hizentra® and Gammanorm® treatment

NCT ID: NCT02053480 Completed - Clinical trials for Pyruvate Kinase Deficiency

Pyruvate Kinase Deficiency Natural History Study

PKD NHS
Start date: December 2013
Phase:
Study type: Observational [Patient Registry]

The purpose of this study is to describe the range and incidence of symptoms, treatments, and complications related to pyruvate kinase deficiency (PKD). Eligible patients are those of all ages with known PKD or with a hemolytic anemia and a family member with PKD. The study will collect retrospective medical history, routine clinical care data, and quality of life measures at baseline and annually for patients with PKD.

NCT ID: NCT01815931 Completed - Emergencies Clinical Trials

Hemolysis in Blood Samples in the ER

Start date: June 2013
Phase: N/A
Study type: Observational

In this study, we aim to identify risk factors for hemolysis in blood samples drawn in the ED.

NCT ID: NCT01770951 Completed - Clinical trials for Atypical Hemolytic Uremic Syndrome (aHUS)

A Retrospective, Observational, Non-interventional Trial to Assess Eculizumab Treatment Effect in Patients With Atypical Hemolytic Uremic Syndrome (aHUS)

Start date: August 31, 2009
Phase:
Study type: Observational

The objective of this retrospective trial is to assess safety and efficacy of eculizumab in aHUS patients treated outside of an Alexion-sponsored controlled clinical trial.

NCT ID: NCT01757431 Completed - Clinical trials for Atypical Hemolytic Uremic Syndrome (aHUS)

The Safety and Efficacy of Eculizumab in Japanese Patients With Atypical Hemolytic Uremic Syndrome (aHUS)

Start date: May 16, 2012
Phase: Phase 2
Study type: Interventional

Protocol is intended to characterize the overall safety and tolerability of eculizumab in this population.

NCT ID: NCT01755429 Completed - Clinical trials for ATYPICAL HEMOLYTIC UREMIC SYNDROME (AHUS)

To Characterize the Safety and Tolerability of Eculizumab in Two Japanese aHUS Patients

Start date: May 2012
Phase: N/A
Study type: Observational

This protocol is intended to formally collect data on the treatment of aHUS with eculizumab in Japanese patients.

NCT ID: NCT01616329 Completed - Hemolysis Clinical Trials

R-FACT Study:Risk Factors for Alloimmunization After Red Blood Cell Transfusions

R-FACT
Start date: January 2009
Phase:
Study type: Observational

Alloantibodies can lead to serious clinical consequences and logistic problems like obtaining properly and timely matched blood for the patients who do develop these antibodies. Prevention of such serious events is possible by extended matching and typing of donor's blood against the patient's for all the possible antigens, but this process is cumbersome and costly. Identifying a high risk group will be a feasible first target for advanced matching a big step forward, and the aim of the investigators study. The aim of the project is to examine the association between clinical, environmental and genetic characteristics of the recipient of erythrocyte transfusions and the risk or resistance to immunization against erythrocyte alloantigens that he/she was exposed to during that transfusion episode.

NCT ID: NCT01406288 Completed - Clinical trials for Escherichia Coli Infections

Outbreak of Hemolytic Uremic Syndrome Linked to Escherichia Coli of Serotype O104:H4

SHU O104 CUB
Start date: July 2011
Phase: N/A
Study type: Observational

The Hemolytic Uremic Syndrome (HUS) in its typical form occurs after a food born infection with a shiga-toxin secreting bacteria, usually Escherichia coli of the O157H7 serotype. An outbreak of bloody diarrhea followed by HUS begun after a collective meal with 120 persons on June 8th, 2011 in Bègles, a city of Bordeaux urban area (CUB). At least 9 patients, 8 adults and 1 child have been involved in this HUS outbreak, E. coli of the O104:H4 serotype being demonstrated in most patients. This outbreak is remarkable by its preponderance in adults and women, its aggressiveness with multiorgan involvement , i.e. the kidneys, brain, liver, pancreas, and skin. Pathophysiology, prognosis, and treatment of typical HUS are poorly defined, particularly in adults who are usually not involved in typical E. coli O157H7 HUS. The aim of the present study is to gain knowledge on these different aspects of the HUS, including response to therapy.