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Acute Leukemia clinical trials

View clinical trials related to Acute Leukemia.

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NCT ID: NCT01603290 Enrolling by invitation - Acute Leukemia Clinical Trials

Change of Fatigue and Physical Fitness in Hospitalized Hematology Patients

Start date: December 2011
Phase: N/A
Study type: Observational

The purposes of this study are to (1) explore the severity of symptom of leukemia patients experienced before and after chemotherapy in hospital, (2) investigate the trajectories of the fatigue and physical fitness, and their related factors, and (3) the correlation between fatigue and physical fitness

NCT ID: NCT01598025 Terminated - Clinical trials for Myelodysplastic Syndrome

Biparental HLA Haplotype Disparate T-cell Depleted Transplants for Patients Lacking an HLACompatible Donor

Start date: May 2, 2012
Phase: N/A
Study type: Interventional

Approximately 30% of patients who are candidates for bone marrow transplants do not have an HLA-matched, or close to matched, donor available. For this reason, doctors have been testing ways to make transplants from HLA-partially matched donors as safe and effective as transplants from HLA-matched donors. This study is being done to test the safety and the treatment results of a specific kind of transplant. In this transplant, blood from two donors will be used. Each donor will share one half of your HLA type. Blood from both donors will be transplanted at the same time.

NCT ID: NCT01557686 Completed - Acute Leukemia Clinical Trials

Health Counseling and Exercise in Patients With Acute Leukemia - Pilot Study

PACE-AL
Start date: May 2010
Phase: Phase 0
Study type: Interventional

The purpose of this pilot study is to test an exercise-based multidimensional intervention for patients with acute leukaemia undergoing consolidation chemotherapy in the context of outpatient management. Further, to test for safety, feasibility and preliminary effect on physical and functional capacity, and health related quality of life.

NCT ID: NCT01509300 Recruiting - Solid Tumors Clinical Trials

HLA-haploidentical Hematopoietic Stem Cell Transplantation for Children and Adolescents With Acute Leukemia, Myelodysplastic Syndrome and Solid Tumors

Start date: January 2012
Phase: Phase 1/Phase 2
Study type: Interventional

RATIONALE: Conditioning with total body irradiation (TBI) and fludarabine, cyclophosphamide and anti-thymocyte globulin may induce the engraftment cross the immunologic barrier in the setting of HLA-haploidentical allogeneic hematopoietic cell transplantation. In addition, T-cell depletion may contribute to prevent developing severe acute graft versus host disease (GVHD) in haploidentical transplantation. PURPOSE: This phase I/II trial is to evaluate the safety and efficacy of TBI, fludarabine, cyclophosphamide and antithymocyte globulin with T-cell depleted graft from haploidentical donors in treating patients with acute leukemia and myelodysplastic syndrome.

NCT ID: NCT01502072 Completed - Cancer Clinical Trials

Respiratory Syncytial Virus - RSV Protocol

Start date: December 28, 2011
Phase: Phase 2
Study type: Interventional

The goal of this clinical research study is to learn if ribavirin can help to control RSV in patients with immune systems that have been weakened by a stem cell transplant. Researchers also want to compare the effectiveness of the drug when it is given by mouth to when it is inhaled. The safety of the drug in both methods of delivery will be studied. Ribavirin is designed to prevent the RSV virus from making more copies of itself in the body.

NCT ID: NCT01499147 Completed - Multiple Myeloma Clinical Trials

Fludarabine Based Conditioning for Allogeneic Transplantation for Advanced Hematologic Malignancies

Start date: February 2000
Phase: N/A
Study type: Interventional

New conditioning regimens are still needed to maximize efficacy and limit treatment-related deaths of allogeneic transplantation for advanced hematologic malignancies. Over the past several years, the investigators have evaluated several new conditioning regimens that incorporate fludarabine, a novel immunosuppressant that has limited toxicity and that has synergistic activity with alkylating agents. Recent data have suggested that fludarabine may be used in combination with standard doses of oral or IV busulfan, thus reducing the toxicity previously observed with cyclophosphamide/ busulfan regimens.

NCT ID: NCT01498016 Recruiting - Acute Leukemia Clinical Trials

Pharmacokinetic Study of Busulfan in Allogeneic Stem Cell Transplantation in Adult Patients With Acute Leukemia

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

Intravenous Busulfan (iv-Bu) is commonly used as part of preparation regimen for allogeneic hematopoietic stem cell transplantation for patients with acute leukemia. Though the pharmacokinetics data are available for population from America, Europe and Japan or Korea in Asia, there are no data in Chinese population. It is shown that high Bu concentration are associated with the toxicity such as veno-occlusion disease and lower concentration is correlated with reduced anti-leukemia effect, thus the monitoring of Bu and/or the strategy to achieve an optimal target Bu concentration are accepted to avoid toxicity while maintain the anti-leukemia effect which may overall improve the outcome of allo-SCT. Thus we conduct the pharmacokinetic study in Chinese population.

NCT ID: NCT01496547 Completed - Acute Leukemia Clinical Trials

Sequential Intensive Chemotherapy Followed by RIC for Refractory and Relapse AML

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

Patients with refractory and relapse leukemia had poor outcome even with allogeneic stem cell transplantation. In our previous retrospective study, the overall survival is 14.6+/-8.8% while 90% patients eventually relapsed with marrow ablative conditioning mostly standard iv-Bu-Cy or Cy-TBI. The accumulated TRM is 29.5+/-11.5%. Thus our data suggested that the conventional transplantation approach may not be able to overcome the refractory disease. A new strategy to combined a low dose regimen following intensive chemotherapy for tumor reduction seems to be effect in both relapsed. high-risk and refractory AML or ALL. In this study, we focus on a new treatment strategy for particular refractory AML patients.

NCT ID: NCT01472055 Recruiting - Acute Leukemia Clinical Trials

Pharmacokinetic Study of Fludarabine in Pediatric Hematopoietic Stem Cell Transplantation

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

The purpose of this study is to analysis of the pharmacokinetics of fludarabine for hematopoietic stem cell transplantation in pediatric patients.

NCT ID: NCT01404520 Completed - Acute Leukemia Clinical Trials

Patient Activation, Counseling and Exercise - Acute Leukemia (PACE-AL)

PACE-AL
Start date: June 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to test a new preventive and restorative intervention for patients with acute leukaemia undergoing consolidation chemotherapy, to measure and delineate the patients' treatment related symptom burden and to explore the effect of the intervention on length of hospital stay, duration of sick leave and return to work status. Further, to examine the relationship of the symptom profile with clinical indicators, physiological response, physical performance and survival.