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Iron Deficiency clinical trials

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NCT ID: NCT05477498 Withdrawn - Iron-deficiency Clinical Trials

Iron Substitution With Ferric Carboxymaltose as Treatment Strategy for Heart Failure Patients With Preserved Ejection Fraction

IRON-HFpEF
Start date: December 1, 2021
Phase: Phase 4
Study type: Interventional

This study aims to investigate the effects of treatment with intravenous ferric carboxymaltose on exercise tolerance measured as VO2peak in patients with HFpEF and iron deficiency, compared to placebo.

NCT ID: NCT04855266 Withdrawn - Iron-deficiency Clinical Trials

Iron Sucrose in Patients With Iron Deficiency and POTS

Start date: April 2021
Phase: Phase 2
Study type: Interventional

This study aims to investigate whether the treatment of non-anemic iron deficiency with intravenous iron sucrose will result in decreased symptom reporting and improved cardiovascular indices in patients with Postural Orthostatic Tachycardia syndrome (POTS).

NCT ID: NCT03873584 Withdrawn - Anemia Clinical Trials

Improvement of Fatigue Symptoms in the Iron Deficiency Anemia With Iron Succinylate Therapy

IFAISTOS
Start date: September 1, 2022
Phase:
Study type: Observational

The treatment of anemia depends on its cause. Patients with underlying iron-deficient anemia should be treated or referred to a specialist (eg gynecologist, gastroenterologist) for treatment.deficiency anemia are global health problems and common medical conditions seen in everyday clinical practice. Iron is vital for biological functions, such as breathing, energy production, DNA synthesis, and cell proliferation. Iron deficiency refers to the reduction of iron stores and precedes the occurrence of iron deficiency anemia. Iron deficiency anemia is a more severe condition in which low levels of iron are associated with anemia and the presence of small cellular red blood cells.

NCT ID: NCT03800446 Withdrawn - Iron-deficiency Clinical Trials

Validation of a Point-of-care Device Measuring Ferritin With Capillary Blood

FerPOC
Start date: September 2019
Phase: N/A
Study type: Interventional

Measurement of iron is important for identifying both low and high iron levels in the body. Measuring a protein in the blood called ferritin is currently the easiest way to determine a patient's iron status. However, the test requires a blood sample that is be sent to the laboratory for measurement, which can cause delays in obtaining the result. The investigators are testing whether a point of care device that measures ferritin levels using a capillary blood sample is accurate compared to current methods of testing. This could allow measurement of ferritin immediately in the clinic with only a drop of blood, and enable treatment decisions based on these results.

NCT ID: NCT03073369 Withdrawn - Anemia Clinical Trials

Effect of Ergocalciferol on Iron Metabolism in Individuals With Chronic Kidney Disease

Start date: January 1, 2018
Phase: Phase 4
Study type: Interventional

The purpose of the study is to learn more about how treatment with vitamin D can affect iron metabolism and blood levels of hepcidin (hormone controlling iron levels) in people with chronic kidney disease (CKD). Iron is an essential mineral which is a major component of proteins that carry oxygen in the blood. Problems with iron metabolism can lead to low blood levels (anemia), which can commonly happen in people with CKD. New research over the last decade has uncovered a new hormone called `hepcidin', which is made in the liver and released into the blood. Hepcidin controls how much iron is in the blood by preventing the absorption of iron from food. Blood levels of hepcidin C are found to be high in people with CKD, and a recent small study in people with normal kidney function showed that treatment with vitamin D decreased hepcidin levels. In this study, investigators would like to examine the effects of vitamin D (Ergocalciferol) on iron metabolism and blood levels of hepcidin in individuals with CKD.

NCT ID: NCT02977611 Withdrawn - Iron Deficiency Clinical Trials

The Safety of a High-Dose, Rapid Infusion of Iron Sucrose

Start date: January 2017
Phase: Phase 2
Study type: Interventional

Iron sucrose infusion is an iron replacement used to treat iron deficiency anemia (not enough iron in the body to make hemoglobin). Iron is a mineral that the body needs to produce hemoglobin, which carries oxygen in the blood. When the body does not get enough iron, it cannot produce enough hemoglobin and you become anemic. The research study is looking at the side effects of using a higher dose and faster rate of iron sucrose infusion than what is used in standard of care. The purpose of this study is to see if infusion with 500 mg of iron sucrose over a one hour time period can be done safely. If this can be done safely, it may reduce the total number of infusions required and the time for each infusion. This may be less costly and less burdensome to patients.

NCT ID: NCT01865175 Withdrawn - Iron Deficiency Clinical Trials

A Pilot Study Comparing Tolerance of Oral Heme Iron Polypeptide With Oral Ionic Iron

Start date: January 2016
Phase: Phase 4
Study type: Interventional

This is a pilot study designed to compare the tolerance of ionic iron (ferrous sulphate) with heme iron polypeptide. Subjects will take one week of one product followed by a week with no product followed by a week with the other product. Subjects will complete a daily diary to assess side effects. Hypothesis: Heme iron polypeptide is associated with fewer gastrointestinal side effects than ionic iron.