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Hematologic Diseases clinical trials

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NCT ID: NCT02487563 Completed - Thrombocytopenia Clinical Trials

Prospective Study of Patients With Thrombocytopenia Following HSCT

Start date: October 2015
Phase: Phase 3
Study type: Interventional

Isolated thrombocytopenia is a common and severe complication of HSCT, which often leads to an increased risk of life-threatening hemorrhage, frequent requirement of platelet transfusions and extended hospital stays, representing a challenging clinical problem. Current treatments for thrombocytopenia after HSCT are frequently unsatisfactory in platelet recovery and for preventing potentially fatal bleeding complications. Therefore, it is urgent to explore an effective therapy to improve the outcomes of thrombocytopenia after HSCT. Previous studies have demonstrated that decitabine, a hypomethylating agent, may reduce platelet transfusions in myelodysplastic syndrome (MDS) patients. The investigators conducted an prospective clinical trial to evaluate the safety and efficiency of rhTPO and decitabine in the treatment of thrombocytopenia following HSCT.

NCT ID: NCT02484053 Completed - Oncologic Disorders Clinical Trials

Rapid Infusion Rituximab, Hematologic, Oncologic, and Rheumatologic Disorders

Start date: June 2015
Phase: Early Phase 1
Study type: Interventional

Rituximab is frequently used in adult and pediatric cancers, blood disorders, lymphoma (a cancerous growth made up of lymphoid tissue), graft-versus-host-disease (complication that can occur after a stem cell or bone marrow transplant), diseases of the immune system (the cells and substances that protect the body from infection) and rheumatologic conditions. Rituximab works by decreasing or temporarily eliminating a specific type of white blood cell, the B-lymphocyte. Overall, rituximab is generally well tolerated. The likelihood of an infusion-related reaction, or symptoms such as fever, chills, hives, low blood pressure or swelling, is very low, but highest during a patient's first infusion of rituximab and decreases with each additional dose. Adults commonly receive rituximab at a faster rate if they have done well with the first infusion, this study will help determine if the same approach is well tolerated in children. In this study, the investigators are testing a new method of administering rituximab which may reduce the time it takes to receive the medication. The initial ordered amount of rituximab will not change from the current standard of care (meaning what is usually done by doctors, and would likely be done if you were not on this study). The period of time over which rituximab is given is what is being studied.

NCT ID: NCT02483325 Completed - Clinical trials for Hematological Diseases

Study Evaluating the Efficacy of Allogeneic Transplant Conditioning With Adaptive Dose Busulfan Intravenous (Busilvex®) in Patients at High Risk of Carrying Blood Diseases

BX-PK
Start date: September 2014
Phase: Phase 2
Study type: Interventional

Determine the efficiency of a myéloablative conditioning associating Fludarabine, Thymoglobuline, and intravenous Busulfan with adapted dose, according to a pharmacokinetics realized in the first day of administration (or J-6 of the conditioning) of the busulfan, in preparation for a allogenic transplant family or not family compatible HLA.

NCT ID: NCT02461199 Recruiting - Blood Disorders Clinical Trials

Stool Transplantation to Reduce Antibiotic Resistance Transmission

START
Start date: February 2015
Phase: N/A
Study type: Observational

During this prospective observational study, the investigators collect the information about the outcomes of fecal microbiota transplantation in patients with blood disorders, performed to eradicate gut colonization with multidrug-resistant (MDR) bacteria. Patients with blood disorders are characterized by poor diversity of gut microbiome, affected by repeated chemotherapy and antimicrobial treatments. This makes them vulnerable to colonization by pathogenic bacteria carrying genes responsible for antibiotic resistance. In case of gut mucosa injury and severe immune suppression, these colonizing bacteria may cause severe systemic infections. As the bacteria are secreted with the stool, the colonized patients become an epidemiologic threat to the others. Fecal microbiota transplantation (FMT) was shown to be very efficient in treatment of relapsed and refractory Clostridium difficile infection and became a standard treatment. In home institution, the investigators use FMT not only in case of Clostridium difficile colitis, but also in case of gut colonization with multidrug-resistant (MDR) bacteria. This is based on assumption that physiological gut flora may outcompete the pathogenic bacteria similarly as in case of Clostridium difficile and lead to loss of colonization. The procedure is performed in all patients colonized, who qualify according to listed inclusion and exclusion criteria .

NCT ID: NCT02456818 Enrolling by invitation - Clinical trials for Hematological Disease

Assessing the Effect of Contact Isolation on Nosocomial Colonization With ESBL-EC in German Hematology/Oncology Wards

CONTAIN
Start date: January 2015
Phase: N/A
Study type: Observational

This study aims to evaluate the impact of contact isolation on the rate of hospital-acquired transmissions of ESBL-producing Escherichia coli (ESBL-EC) and the rate of colonization and infection. On the basis of this study, it will be possible to re-evaluate the need for contact isolation for patients colonized or infected with ESBL-EC.

NCT ID: NCT02447237 Completed - Clinical trials for Delayed Gastric Emptying

Randomized Trial:the Effect of Liquid Food on the Intake of Energy and Protein in Malignant Hematologic Patients

Start date: March 2015
Phase: N/A
Study type: Interventional

The study investigates the effect of liquid food on the intake of energy and protein compared to solid food. One group will receive dietary counselling in fulfilling their need for energy and protein from liquid food and the other group from solid food.

NCT ID: NCT02442011 Recruiting - Clinical trials for Hematological Disorders

Hematology Biobank : Invitro Study of Blood Disorders

Start date: January 2014
Phase:
Study type: Observational

This is a bio repository of blood specimens from subjects with different Hematological disorders.

NCT ID: NCT02435316 Completed - Clinical trials for Hematologic Diseases

Comparison of Educational Methods for Teaching Peripheral Blood Smears

PBS
Start date: April 2012
Phase: N/A
Study type: Interventional

This is a prospective, randomized controlled, crossover trial comparing the effectiveness one two curricular designs to teaching peripheral blood smears to residents.

NCT ID: NCT02380378 Recruiting - Clinical trials for Hematologic Diseases

Registry of Philadelphia-Negative Myeloproliferative Neoplasms

MPN
Start date: March 2015
Phase:
Study type: Observational [Patient Registry]

This study was developed to document current diagnosis and treatment patterns, clinical outcomes, and health care resource use associated with Philadelphia-Negative Myeloproliferative Neoplasms, in the different risk classifications for each disease.

NCT ID: NCT02343965 Completed - Clinical trials for Hematologic Diseases

The Impact of the Practice of Touch-massage on the Anxiety of Patients With Hematological Disorders Hospitalized in a Protective Environment, a Randomized, Controlled Study

TANDHEMS
Start date: January 2015
Phase: N/A
Study type: Interventional

Each year, 17000 cases of severe hematological diseases are diagnosed in France, with more than 6,000 of these requiring hospitalization in a protective, sterile environment. New methods, such as touch massage, have emerged in response to anxiety symptoms observed in patients in such sterile and isolated surroundings. We hypothesize that during the period of isolation, touch massage becomes a nursing care which can help the patient.