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Iron Deficiency clinical trials

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NCT ID: NCT03840031 Completed - Clinical trials for Iron Deficiency Anemia

Iron Bioavailability From Biofortified Orange-fleshed Sweet Potato

SASHA-II
Start date: March 25, 2019
Phase: N/A
Study type: Interventional

To combat iron deficiency in Low and Middle-Income Countries, sustainable food-based solutions have to be implemented to serve populations, not only individuals. One solution is the introduction of iron biofortified staple crops on market level. Before market level introduction, the bioavailability of iron in the new biofortified Orange Fleshed Sweet Potato (OFSP) breed needs to be assessed. In this study the investigator compares the fractional and total iron absorption after extrinsic stable isotope labelling of the new biofortified high iron OFSP variety and a normal market level OFSP variety. The study is conducted in Malawian women of reproductive age with marginal iron status.

NCT ID: NCT03835377 Completed - Anemia Clinical Trials

Iron-Biofortified Beans Intervention in Mexico

Start date: January 6, 2010
Phase: N/A
Study type: Interventional

The objective of this cluster-randomized efficacy feeding trial was to determine the effects of consuming iron-biofortified beans (Fe-Beans) on iron status in children, compared to control beans (Control-Beans). A cluster-randomized trial of biofortified beans (Phaseolus vulgaris L), bred to enhance iron content, was conducted for 6 months.

NCT ID: NCT03819530 Completed - Clinical trials for Iron Deficiency Anemia

Child of Urban Poverty Iron Project (CUPIP) - A Pilot Study

CUPIP
Start date: September 16, 2019
Phase: N/A
Study type: Interventional

The first 1,000 days of life are critical periods for brain development. Proper nutrition lays the foundation for optimal growth, health, and neurodevelopment across the lifespan. Poor nutrition in this vulnerable period has irreversible consequences, including stunting, susceptibility to sickness, reduced school performance and productivity, and impaired intellectual and social development. UNICEF reported in 2018 that among the low cost flat residents in urban areas of the Klang Valley, 15% of children under 5 years old were stunted, 22% underweight, and 23% either overweight or obese. Will a micronutrient supplementation program improve the growth and iron status of children aged 6 months to 5 years staying in Lembah Subang? Children will be randomized into treatment and control groups. Treatment groups will receive dietary micronutrient supplementation packets. Measurements of height and weight and iron status will be taken at baseline and 4 months later.

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: NCT03793959 Completed - Iron-deficiency Clinical Trials

How Does a Synbiotic Supplement Affect Iron Status During Iron Repletion in Iron Depleted Female Athletes?

Start date: August 28, 2016
Phase: N/A
Study type: Interventional

Iron deficiency (ID) affects ~30% of female athletes, and its consequences are highly relevant to athletic performance. Poor iron (Fe) uptake remains a major factor in the development of ID. While animal studies suggest that prebiotics may improve Fe uptake, this has not been well-studied in humans. The main objective of the proposed study is to determine the effects of synbiotic supplementation on the Fe status of ID female athletes during Fe repletion.

NCT ID: NCT03769441 Active, not recruiting - Iron-deficiency Clinical Trials

Effect of Ferric Carboxymaltose on Exercise Capacity After Kidney Transplantation

EFFECT-KTx
Start date: August 2, 2019
Phase: Phase 3
Study type: Interventional

Iron deficiency is common in kidney transplant recipients and is associated with impaired exercise tolerance and an unfavourable prognosis. This multicentre double-blind, placebo-controlled randomized controlled clinical trial will allow the investigators to analyse the effects of intravenous iron correction with ferric(III) carboxymaltose on exercise tolerance and other parameters, in comparison to a placebo.

NCT ID: NCT03762148 Completed - Iron-deficiency Clinical Trials

Determination of a Dose-dependent Effect of GOS on Iron Absorption, and Addition of Vitamin C

Fe_GOS_2
Start date: April 1, 2019
Phase: N/A
Study type: Interventional

Iron deficiency is still the most common and widespread nutritional disorder in the world according to WHO. In a recent iron absorption study in adult women with low iron stores in our lab (publication under review), we found that 15 g of GOS given with an iron supplement in the form of iron fumarate acutely increased iron absorption when given with water and a bread based meal. The dose of 15 g of GOS was tolerated well by the participants. As a follow up to the study mentioned above, we want to investigate: 1) if acute iron absorption is affected by lower doses of GOS; 2) whether this acute effect occurs for other commonly used iron compounds as well, such as iron sulphate and iron phosphate; and 3) if there are potential interactions on absorption with other enhancers of iron absorption, such as vitamin c.

NCT ID: NCT03749603 Completed - Anemia Clinical Trials

A Study Assessing Iron Status and Anemia in Filipino School Children From MIMAROPA Region

Start date: January 14, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to assess the iron status and to confirm the usability of the non-invasive ZnPP measurement for screening the different stages of iron deficiency defined by standard measurements from blood.

NCT ID: NCT03748043 Recruiting - Iron-deficiency Clinical Trials

the Effectiveness of Lactoferrin in Treatment of Iron Deficiency Anemia in Children With Chronic Tonsillitis

Start date: February 21, 2019
Phase: Phase 4
Study type: Interventional

the investigators will compare the response to iron deficiency anemia to lactoferrin plus ferrous poly maltose versus ferrous poly maltose in Children With Chronic Tonsillitis

NCT ID: NCT03707249 Completed - Iron-deficiency Clinical Trials

Iron Status and Cardiopulmonary Physiology

Start date: January 19, 2016
Phase: N/A
Study type: Interventional

This study involved human volunteers undertaking a high-altitude expedition. It assessed changes in physiological parameters of relevance to high-altitude cardiopulmonary physiology. Participants included a subgroup of those taking part in an existing adventurous training expedition and were randomised in a 1:1 fashion to receive either intravenous iron or normal saline several weeks prior to departure. During the expedition, participants were investigated by means of transthoracic echocardiography, peripheral oxygen saturation measurement and heart rate monitoring and through the drawing of venous blood samples. Bloods were later analysed for markers of iron status.