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Anemia clinical trials

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NCT ID: NCT03025698 Active, not recruiting - Aplastic Anemia Clinical Trials

A Phase II Dose-escalation Study Characterizing the PK of Eltrombopag in Pediatric Patients With Previously Untreated or Relapsed Severe Aplastic Anemia or Recurrent Aplastic Anemia

Start date: September 30, 2017
Phase: Phase 2
Study type: Interventional

This is a phase II, open label, multi-center, intra-patient dose escalation study to characterize the pharmacokinetics (PK) after oral administration of eltrombopag in combination with immunosuppressive therapy in pediatric patients with previously untreated or relapsed/refractory severe aplastic anemia or recurrent aplastic anemia.

NCT ID: NCT02959125 Active, not recruiting - Pregnancy Clinical Trials

NutFish and Nutrient Supplementation in Pregnancy Class to Improve Maternal and Birth Outcomes

Start date: December 12, 2016
Phase: N/A
Study type: Interventional

This study evaluates the intervention of Nut Fish based food, micro nutrients supplementation and pregnancy class to improve maternal and birth outcome. This is cluster randomized trial with two arms. The intervention group will receive Nut Fish based supplementation, multiple micro nutrients, and pregnancy class. The control group will receive government food supplementation, iron folic acid supplementation, and pregnancy class.

NCT ID: NCT02874326 Active, not recruiting - Anemia Clinical Trials

Octreotide in Patients With GI Bleeding Due to Rendu-Osler-Weber

ROW
Start date: October 2016
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine whether long-acting octreotide is safe and effective in the treatment of patients with Rendu-Osler-Weber (e.g. HHT). The study hypothesis is that octreotide is safe and will reduce transfusion requirements and endoscopy frequency in ROW patients with refractory anaemia due to bleeding gastrointestinal telangiectasias.

NCT ID: NCT02845596 Active, not recruiting - Clinical trials for Severe Aplastic Anemia

Unrelated Donor Transplant Versus Immune Therapy in Pediatric Severe Aplastic Anemia

Start date: August 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the feasibility of comparing outcomes of patients treated de novo with immunosuppressive therapy (IST) versus matched unrelated donor (MUD) hematopoietic stem cell transplant (HSCT) for pediatric acquired severe aplastic anemia.

NCT ID: NCT02769845 Active, not recruiting - Sickle Cell Anemia Clinical Trials

SACRED A Prospective Research Study to Reduce Stroke in Children With Sickle Cell Anemia

SACRED
Start date: March 16, 2016
Phase: N/A
Study type: Interventional

Prospective screening and treatment study for children with Sickle Cell Anemia and increased stroke risk living in the Dominican Republic.

NCT ID: NCT02566304 Active, not recruiting - Clinical trials for Acute Myeloid Leukemia

Reduced Intensity Chemotherapy and Radiation Therapy Before Donor Stem Cell Transplant in Treating Patients With Hematologic Malignancies

Start date: November 13, 2015
Phase: Phase 2
Study type: Interventional

This clinical trial studies the use of reduced intensity chemotherapy and radiation therapy before donor stem cell transplant in treating patients with hematologic malignancies. Giving low doses of chemotherapy, such as cyclophosphamide and fludarabine phosphate, before a donor stem cell transplant may help stop the growth of cancer cells. It may also stop the patient's immune system from rejecting the donor's stem cells. The donated stem cells may replace the patient's immune cells and help destroy any remaining cancer cells (graft-versus-tumor effect). Reducing the intensity of the chemotherapy and radiation may also reduce the side effects of the donor stem cell transplant.

NCT ID: NCT02541708 Active, not recruiting - Clinical trials for Iron-Deficiency Anemia

IV Ferric Carboxymaltose Compared With Oral Iron in the Treatment of Iron Deficiency Anemia at Delivery in Tanzania

Ferinject
Start date: September 2015
Phase: Phase 3
Study type: Interventional

Intravenous iron preparations have been shown to be superior to oral iron and have largely replaced the treatment of anaemia in Northern countries. However, the socio-economic and medical conditions in low resource countries greatly differ from those in northern countries. Patients' different access to medication supply, perception of medication need and compliance as well as the burden of concomitant disease like malaria, soil-transmitted helminths, schistosomiasis, HIV and red blood cells (RBC) genetic disorders may influence effectiveness and safety of iron substitution modality. The aim of the present study is to compare iv iron substitution by ferric carboxymaltose (Ferinject®) to per oral iron substitution in a low resource country

NCT ID: NCT02385409 Active, not recruiting - Anemia Clinical Trials

Incidence and Reasons for Preoperative Anemia in Elective Lower Joint Arthroplasty

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

Preoperative anemia is an independent risk factor for the need for allogeneic transfusion during surgery and increased postoperative morbidity. Treatment of preoperative anemia is recommended. However the type of preoperative anemias in elective hip- and knee surgery has only been sparsely studied. This observational study aims to investigate the incidence and type of anemias prior to elective hip- and knee arthroplasty.

NCT ID: NCT02048813 Active, not recruiting - Anemia Clinical Trials

Ibrutinib and Rituximab Compared With Fludarabine Phosphate, Cyclophosphamide, and Rituximab in Treating Patients With Untreated Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma

Start date: February 20, 2014
Phase: Phase 3
Study type: Interventional

This phase III trial studies ibrutinib and rituximab to see how well they work compared to fludarabine phosphate, cyclophosphamide, and rituximab in treating patients with untreated chronic lymphocytic leukemia or small lymphocytic lymphoma. Ibrutinib may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Chemotherapy drugs, such as fludarabine phosphate and cyclophosphamide, work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Rituximab is a monoclonal antibody. It binds to a protein called CD20, which is found on B cells (a type of white blood cell) and some types of cancer cells. This may help the immune system kill cancer cells. It is not yet known whether fludarabine phosphate, cyclophosphamide, and rituximab may work better than ibrutinib and rituximab in treating patients with untreated chronic lymphocytic leukemia or small lymphocytic lymphoma.

NCT ID: NCT01995331 Active, not recruiting - Aplastic Anemia Clinical Trials

Moderate-dose Cyclophosphamide for Childhood Acquired Aplastic Anemia

Start date: March 2012
Phase: Phase 4
Study type: Interventional

Severe aplastic anemia (SAA)is characterized by the depletion of hematopoietic precursors associated with life-threatening complications. High-dose cyclophosphamide has been found to yield a complete response (CR) in adults and children with SAA.However, the optimal dosage of cyclophosphamide for patients in childhood remains unclear. So we explore the ideal dosage of cyclophosphamide for the treatment of children with SAA.