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Iron Deficiency Anemia Treatment clinical trials

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NCT ID: NCT04744181 Completed - Anemia Clinical Trials

Patient Blood Management In CARdiac sUrgical patientS

ICARUS
Start date: January 18, 2021
Phase:
Study type: Observational

Nowadays up to 40% of patients undergoing cardiac surgery receives at least 1 unit of red blood cell transfusion during surgery or during the first week after surgery. Moreover up to 40% of these patients shows an absolute or relative iron deficiency, with or without anaemia. The objective of this study is to assess whether to implement an adequate correction of iron according to current "patients blood management" recommendations might reduce RBC transfusion requirements in patients undergoing heart surgery. Data obtained in patients included in the study will be compared to those of a case-control population selected from patients consecutively treated at the same department in the previous 2 years.

NCT ID: NCT04705662 Completed - Clinical trials for Iron Deficiency Anemia

GI Effects of Iron in Healthy Volunteers

Start date: March 1, 2021
Phase: N/A
Study type: Interventional

Over recent years there has been a lot of research looking at how the bacteria in our gut affects our health. Some medications are known to cause changes in gut bacteria. Many patients that are prescribed iron report gastrointestinal side effects. This research project aims to see if the cause of the gastrointestinal side effects is due to iron causing changes in the gut bacteria. This can be detected via measuring the levels of hydrogen and methane and other compounds in the breath and stool.

NCT ID: NCT04631679 Completed - Anemia Clinical Trials

Investigation of the Wash-out Effect of Intravenous Iron by Cell Savers (WASH-OUT)

WASH-OUT
Start date: November 8, 2019
Phase:
Study type: Observational

The study is a pilot study, which involves cardiothoracic patients. Patients, who are scheduled for elective cardiosurgical procedure, will be seen in multidisciplinary anesthesia/Patient Blood Management (PBM) clinic and screened for anemia prior to surgery. Anemic patients will eventually be treated with 500mg of ferric carboxymaltose 1 to 4 days prior to surgery. A high blood loss is expected in these procedures (>500ml). Blood is collected and re-transfused to the patient via use of cell savers/ autologous blood restoration. The investigators will examine how fast intravenous ferric carboxymaltose is stored within the iron storage cells of the body, and how much remains within the patients blood at the time point of surgery. Next, the investigators will assess the wash out effect of iron via cell salvage. The hypothesis of this trial is that ferric carboxymaltose is washed out of the collected patient's blood by cell caver usage (Wash-Out Effect).

NCT ID: NCT04267653 Completed - Clinical trials for Iron Deficiency Anemia Treatment

Lactoferrin Efficacy Versus Ferrous Sulfate in Treatment of Patients With Iron Deficiency Anemia

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

Lactoferrin (Lf) is a mammalian cationic iron binding glycoprotein belonging to the transferrin family which was discovered 70 years ago, and isolated simultaneously from human and bovine milks in 1960. It is widely distributed in all biological fluids and is also expressed by immune cells, which release it under stimulation by pathogens

NCT ID: NCT03610230 Terminated - Clinical trials for Iron Deficiency Anemia Treatment

Iron Isomaltoside Compared With Iron Sucrosein Peritoneal Dialysis Patients

Start date: February 1, 2019
Phase: N/A
Study type: Interventional

1. To compare patient-reported satisfaction, efficacy and short-term safety profile of Monofer® in a single bolus dose with Venofer® in split doses in the treatment of absolute or functional iron deficiency anemia in patients on PD. 2. To compare patient symptomatology on fatigue after treatment of Monofer® compared with Venofer® .

NCT ID: NCT01227616 Completed - Clinical trials for Iron Deficiency Anemia Treatment

Compare Efficacy/Safety of Repeat Doses of Ferumoxytol With Iron Sucrose in CKD Subjects With IDA and on Hemodialysis

Start date: August 2013
Phase: Phase 4
Study type: Interventional

The objectives of this study are to compare the efficacy and safety of repeat doses of intravenous (IV) ferumoxytol with IV iron sucrose for the treatment of IDA in subjects with hemodialysis-dependent CKD.