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Anemia clinical trials

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NCT ID: NCT01732445 Completed - Anemia Clinical Trials

Ruxolitinib Phosphate and Danazol in Treating Anemia in Patients With Myelofibrosis

Start date: April 2013
Phase: Phase 2
Study type: Interventional

This phase II pilot trial studies how well ruxolitinib phosphate and danazol work in treating anemia in patients with myelofibrosis. Ruxolitinib phosphate and danazol may cause the body to make more red blood cells. They are used to treat anemia in patients with myelofibrosis.

NCT ID: NCT01725789 Completed - Anemia Clinical Trials

Ferinject® Assessment In GastRectomy Patients With Acute Isovolemic Anemia (FAIRY)

Start date: November 2012
Phase: Phase 3
Study type: Interventional

This study is designed to evaluate the efficacy of Ferinject® in improving acute isovolemic anemia after gastrectomy for gastric cancer in terms of Quality of life(QOL )and objective measures (Hb and iron parameters). Furthermore, the tolerability and safety of Ferinject® treatment will be evaluated.

NCT ID: NCT01720147 Completed - Fanconi Anemia Clinical Trials

Quercetin in Children With Fanconi Anemia; a Pilot Study

Start date: July 2012
Phase: Phase 1
Study type: Interventional

Fanconi anemia (FA) is an autosomal recessive disease characterized by progressive bone marrow failure (BMF), congenital abnormalities and a predisposition to malignancy.

NCT ID: NCT01719146 Completed - Clinical trials for Anemia of End Stage Renal Disease

Prospective Observational Study of Erythropoietin-Iron Interaction in Anemia of Renal Disease

Start date: January 2013
Phase:
Study type: Observational

The purpose of this study is to prospectively collect data on doses of Erythropoietic Stimulating Agents (ESA) and Intravenous Iron, and the markers of erythropoietic activity and iron status. These data will be used to derive mathematical models which will subsequently guide dosing of both agents, such that a desired therapeutic outcome is achieved in every patient, while minimizing patient exposure to both agents.

NCT ID: NCT01716923 Completed - Clinical trials for Focus:Use of S303 RBCs in Patients With Acute Anemia

Study to Assess S303 RBCs and Evaluate Safety and Efficacy in Patients Requiring Transfusion Support of Acute Anemia

Start date: April 2013
Phase: Phase 3
Study type: Interventional

The clinical study will assess the in-vitro characteristics of red blood cells (RBCs) per the European Union (EU) criteria for leukocyte depleted RBCs in additive solution and evaluate the safety and efficacy of S-303 treated RBCs in a patient population requiring RBC transfusion support for acute anemia.

NCT ID: NCT01716559 Completed - Anemia Clinical Trials

An Observational Study of NeoRecormon (Epoetin Beta) in Anemic Patients With Non-myeloid Malignancy

Start date: August 2010
Phase: N/A
Study type: Observational

This observational, prospective, multicenter study will evaluate the treatment response rate and the safety of NeoRecormon (epoetin beta) in anemic patients with non-myeloid malignancy. In addition to NeoRecormon, patients receive chemotherapy for their malignancy. Data will be collected for 16 weeks.

NCT ID: NCT01712308 Completed - Anemia Clinical Trials

Sotatercept in Treating Patients With Myeloproliferative Neoplasm-Associated Myelofibrosis or Anemia

Start date: February 21, 2013
Phase: Phase 2
Study type: Interventional

This phase II trial studies the side effects of and how well sotatercept works in treating patients with myeloproliferative neoplasm-associated myelofibrosis or anemia. Sotatercept may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.

NCT ID: NCT01703169 Completed - Clinical trials for Severe Aplastic Anemia

Efficacy and Safety of Eltrombopag In Patients With Severe and Very Severe Aplastic Anemia

Start date: November 2012
Phase: Phase 2
Study type: Interventional

The investigators hypothesis is that eltrombopag given to patients with moderate to very severe aplastic anemia will result in an increase in platelet counts. The investigators hypothesize that in patients with moderate to very severe aplastic anemia, treatment with eltrombopag will lead to fewer platelet transfusions, red blood cell transfusions, and fewer bleeding events. The investigators hypothesize that in patients with moderate to very severe aplastic anemia, eltrombopag will have an acceptable toxicity rate <3%, at doses that result in increased platelet counts. Finally the investigators hypothesize that plasma eltrombopag levels in peripheral blood will correlate with improved platelet counts.

NCT ID: NCT01703104 Completed - Sickle Cell Anemia Clinical Trials

The Efficacy of Jobelyn (Sorghum Bicolor Extract)in the Treatment of Sickle Cell Anemia

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

The primary objective is to determine if there is a significant increase in the haematocrit value of patients on Jobelyn and standard therapy compared to those on standard therapy alone.

NCT ID: NCT01701310 Completed - Anemia Clinical Trials

IVICA: Intravenous Iron in Colorectal Cancer Associated Anaemia

IVICA
Start date: April 2012
Phase: Phase 4
Study type: Interventional

116 eligible patients with confirmed non-metastatic colorectal adenocarcinoma and anemia will be randomized to receive either oral ferrous sulphate (control) or intravenous ferric carboxymaltose (intervention). It is hypothesized that intravenous iron supplementation is more efficacious than oral iron therapy.