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Anemia, Iron Deficiency clinical trials

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NCT ID: NCT00971672 Completed - Healthy Infants Clinical Trials

Incidence of Iron Deficiency Anemia in Toddlers

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

The frequency of iron deficiency anemia was extensively studied in infants on the first year of life. There is not enough information about the frequency of iron deficiency during the second and third years of life. In a previous study performed in Israel and published in Pediatrics 2006 the incidence of anemia does not decrease towards age 18 months. Then there is reasonable to study the iron deficiency frequency beyond this age.

NCT ID: NCT00907088 Completed - Iron Deficiency Clinical Trials

Nutritional Education and the Prevention of Iron Depletion in Children 9 Months to 2 Years

Start date: January 2006
Phase: N/A
Study type: Interventional

Iron depletion in young children is common and may progress to iron deficiency anemia which is associated with irreversible neurodevelopmental effects. Efforts to prevent iron depletion are key to preventing these effects. In a recent study of 150 young children (12 to 38 months), we found that bottle fed children were almost three times as likely to be iron depleted compared with cup fed children (37% vs 18%). Thus, we hypothesize that an educational intervention designed to encourage timely bottle weaning will lead to a reduction in iron depletion.

NCT ID: NCT00841061 Completed - Iron Deficiency Clinical Trials

Cereals as a Source of Iron for Breastfed Infants

Bfe03B
Start date: July 2003
Phase: N/A
Study type: Interventional

The purpose of this research study is to determine whether the type of iron in infant cereals makes a differance in how well the cereal helps infants remain free of iron deficiency.

NCT ID: NCT00839761 Completed - Anemia Clinical Trials

The Use of Ultra Rice Compared to Iron Drops Consumed by Anemic Children

Start date: December 2006
Phase: N/A
Study type: Interventional

Background: How best to improve iron status among infants in low-income settings is of continued concern in many countries, including Brazil Objective: Design: In a double blind, 5-mo, home-based trial in Brazil, mildly anemic 6 - 24 month-old children (n=175) were randomly assigned to receive either Ultra Rice (URG) fortified with 23,4, mg Fe as micronized ferric pyrophosphate (MFP) and a placebo solution of iron drops, or identical non-fortified rice (CG) and a solution of iron drops. Parents were instructed on the correct dosage of iron drops and to feed their children (including whether and how much rice) as they normally would. Iron status and hemoglobin (Hb) were measured at baseline and at 5 mo.

NCT ID: NCT00810030 Completed - Ulcerative Colitis Clinical Trials

FERINJECT for Correction of Anaemia in IBD Patients, FER-IBD-COR

FER-IBD-COR
Start date: October 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine how safe, tolerable and effective the new standardised dosage regimen of FERINJECT® infusions is, compared with a well established intravenous iron treatment.

NCT ID: NCT00810004 Completed - Clinical trials for Inflammatory Bowel Disease

Maintenance Treatment of Iron Deficiency in IBD Patients

FER-IBD-MAIN
Start date: February 2009
Phase: Phase 3
Study type: Interventional

The aim of this study is to evaluate the treatment of iron deficiency in IBD patients.

NCT ID: NCT00802139 Completed - Clinical trials for Iron Deficiency Anemia

Efficacy and Safety Study of Iron Sucrose and Oral Iron Acetyl-transferrin Hydroglycerin

Start date: February 2008
Phase: Phase 4
Study type: Interventional

multi-center, prospective, randomized, open-labeled, active-drug-controlled, two-parallel-group-comparison(venoferrun group vs Bolgre group)study

NCT ID: NCT00789490 Completed - Iron Deficiency Clinical Trials

Relative Bioavailability of Iron and Folic Acid in New Test Supplement

Start date: October 2005
Phase: Phase 1
Study type: Interventional

Deficiencies of iron and folic acid during pregnancy can lead to adverse outcomes for the fetus, thus supplements are recommended. Adherence to current tablet-based supplements is documented to be poor. Recently a powdered form of micronutrients has been developed which may decrease side-effects and thus improve adherence. However, before testing the efficacy of the supplement as an alternate choice for supplementation during pregnancy, the bioavailability of the iron needs to be determined. The objective of this study is to measure the relative bioavailability of iron and folic acid from a powdered supplement that can be sprinkled on semi-solid foods or beverages versus a traditional tablet supplement in pregnant women.

NCT ID: NCT00760890 Completed - Iron Deficiency Clinical Trials

Iron and the Breast-Fed Infant: Iron Status and Two Regimens of Iron Supplementation

BFe01B1
Start date: June 2001
Phase: N/A
Study type: Interventional

Normal breastfed infants can develop iron deficiency by 6 months of age. This trial tested the hypothesis that regular provision of a source of iron beginning at 4 months of age improves iron status and could prevent iron deficiency. This was a prospective randomized trial involving breastfed infants. To be eligible, infants had to be predominantly breastfed (<200 ml/day of formula) at 4 months of age. At 4 months infants were randomly assigned to one of two interventions or to control. The interventions consisted in the daily administration of medicinal iron in a dose of 7.5 mg (Medicinal Iron Group) or in the daily feeding of one jar of an iron-fortified cereal providing 7 mg of iron each day (Cereal Group). The control group received complementary foods chosen by he parents but no source of iron provided by the investigators. The interventions took place from 4 to 9 months. All infants were subsequently followed to 2 years of age.

NCT ID: NCT00746551 Completed - Anemia Clinical Trials

Intravenous Versus Oral Iron in Late Pregnancy: Results of Treatment

EIVF
Start date: September 2008
Phase: Phase 4
Study type: Interventional

The purpose of this study is to compare the efficacy of body iron storage replenishment between low dose intravenous iron and oral iron in late pregnancy.