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Acute Leukemia clinical trials

View clinical trials related to Acute Leukemia.

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NCT ID: NCT02693899 Completed - Acute Leukemia Clinical Trials

Prospective Study on the Feasibility of Plasma FLT3-Ligand Assay to Achieve a First Estimate of Its Prognostic Value on the Outcome of Patients Treated Intensively for Acute Leukemia

FLAM/FLAL
Start date: May 27, 2016
Phase:
Study type: Observational

Despite advances in their classification and treatment, acute leukemia remain incurable disease for the majority of patients. It is necessary to identify new prognostic markers of survival and new therapeutic targets to improve prognosis. Some studies have shown that Fms-like tyrosine kinase 3-ligand (FLT3-L) could be interesting from this. A more recent study from our group testing a novel therapy in acute lymphoblastic leukemia, showed an increase of this marker in the blood of patients responding to treatment. The aim of our prospective, non-interventional study is to measure the plasma levels of FLT3-L at different times of the management of patients with acute lymphoblastic leukemia but also myeloid. For this, analyzes of the samples collected in the usual care will be conducted to study the relationship between the plasma concentration of FLT3-L and outcomes. If there is any link, the FLT3-L could serve as a predictor of treatment response.

NCT ID: NCT02580071 Completed - Acute Leukemia Clinical Trials

Chinese Herbal Medicine for Immune Reconstitution Following HSCT in Acute Leukemia Patients

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

The treatment options for high-risk acute leukemia patients are limited and these patients are often opt for hematopoietic stem cell transplant (HSCT). However studies show that prognosis following this last-resort therapy is bleak. At times, less than 70% of post-HSCT relapsed AML and ALL patients even achieve complete remission; median overall survival of these cohorts might not reach one year; and 3-year post-HSCT survival rates might be less than 20%. The investigators plan to recruit acute leukemia patients from CMUH which are planned to receive HSCT, and follow the rate and quality of their immune reconstitution. As intervention, part of the patients will receive a Chinese medicine herbal formula, which they will take for 6 months.Differences between the 1-year post-HSCT condition of patients will be examined.

NCT ID: NCT02487069 Completed - Clinical trials for Myelodysplastic Syndrome

Allo-HSCT With Alternative Donor in Treatment of Hematologic Malignancy

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

The purpose of this study is to compare the efficacy of allogeneic hematopoietic stem cell transplantation (allo-HSCT) from matched sibling donor (MSD),matched unrelated donor (MUD) and haploidentical related donors(HRD) in the treatment of hematologic malignancy.

NCT ID: NCT02451592 Completed - Multiple Myeloma Clinical Trials

Fungemia in Hematologic Malignancies

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

The purpose of this study is to determine the risk factors for fungemia in a population of patients diagnosed with hematologic malignancies and eligible for chemotherapy.

NCT ID: NCT02445378 Completed - Depression Clinical Trials

Aromatherapy and Essential Oils in Improving Insomnia and Other Symptoms in Patients With Newly Diagnosed Acute Leukemia Undergoing Chemotherapy

Start date: December 28, 2014
Phase: N/A
Study type: Interventional

This randomized clinical trial studies aromatherapy and essential oils in improving insomnia and other symptoms in patients with newly diagnosed acute leukemia. Aromatherapy and essential oils may help improve insomnia and other complications caused by chemotherapy.

NCT ID: NCT02440178 Completed - Acute Leukemia Clinical Trials

Micafungin Prophylaxis During 1st Induction Chemotherapy for De Novo Acute Leukemia

Start date: September 19, 2015
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether prophylaxis with micafungin is effective in the induction chemotherapy for newly diagnosed acute leukemia patients.

NCT ID: NCT02353559 Completed - Acute Leukemia Clinical Trials

Emotion And Symptom-focused Engagement (EASE): An Intervention for Individuals With Acute Leukemia

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

The purpose of this study is to test the feasibility of an individual psychological and physical symptom intervention, called Emotion And Symptom-focused Engagement (EASE), to reduce traumatic stress and physical symptom burden in individuals newly diagnosed with acute leukemia.

NCT ID: NCT02345850 Completed - Acute Leukemia Clinical Trials

Calcineurin Inhibitor-Free Interventions BMT CTN 1301 for Prevention of Graft-versus-Host Disease (BMT CTN 1301)

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

The study is designed as a three arm randomized Phase III, multicenter trial comparing two calcineurin inhibitor (CNI)-free strategies for Graft-versus-Host Disease (GVHD) prophylaxis to standard tacrolimus and methotrexate (Tac/Mtx) in patients with hematologic malignancies undergoing myeloablative conditioning hematopoietic stem cell transplantation.

NCT ID: NCT02246907 Completed - Acute Leukemia Clinical Trials

Exercise and Quality of Life in Leukemia Patients

EQUAL
Start date: January 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the impact of an exercise intervention on patient-reported anxiety, depression, fatigue, and sleep disturbances among acute leukemia patients. The investigators hypothesize that exercise will reduce fatigue in acute leukemia patients.

NCT ID: NCT02208037 Completed - Clinical trials for Chronic Lymphocytic Leukemia

Novel Approaches for Graft-versus-Host Disease Prevention Compared to Contemporary Controls (BMT CTN 1203)

Start date: August 2014
Phase: Phase 2
Study type: Interventional

Acute Graft-versus-Host-Disease (GVHD) is an important cause of morbidity and mortality after allogeneic hematopoietic stem cell transplantation (HSCT). This study aims to determine if any of three new GVHD prophylaxis approaches improves the rate of GVHD and relapse free survival at one year after transplant compared to the current standard prophylaxis regimen.