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Anemia, Iron Deficiency clinical trials

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NCT ID: NCT00570895 Completed - Iron Deficiency Clinical Trials

Effect of Vitamin C on Iron Absorption

Start date: January 2008
Phase: N/A
Study type: Interventional

Iron deficiency is a common health problem worldwide. Ferrous fumarate (a form of iron) is often added to foods in an effort to prevent iron deficiency. Vitamin C can improve the amount of iron that the body absorbs, therefore it is often added to foods too. However, we don't know if vitamin C really increases the absorption of iron from ferrous fumarate. This study will measure the iron absorption in children from a meal containing some ferrous fumarate with and without vitamin C. The study will include 4 visits to the Children's Nutrition Research Center in Houston, TX.

NCT ID: NCT00558454 Completed - Anemia Clinical Trials

Iron Supplementation of Marginally Low Birth Weight Infants

JOHN
Start date: March 2004
Phase: Phase 4
Study type: Interventional

Iron is essential for brain development and there is a well established association between iron deficiency in infants and poor neurological development. In Sweden, about 5% of newborns have low birth weight (< 2500 g). Due to small iron stores at birth and rapid postnatal growth, they have increased risk of iron deficiency and it is therefore important to prevent iron deficiency in this population. However, excessive iron supplementation can have adverse effects in infants such as growth impairment. In a randomized, controlled trial, we are investigating the effects of 0, 1 or 2 mg/kg/d of iron on brain myelination, cognitive development and growth in low birth weight infants.

NCT ID: NCT00554814 Suspended - Clinical trials for Latent Iron Deficiency

Interest of Biofer ® Compound Used in Blédilait Follow on Milk in Infant With Latent Iron Deficiency

Start date: November 2007
Phase: N/A
Study type: Interventional

The primary purpose of the study is to demonstrate the superiority of Bledilait milk (Biofer® 2mg/100kcal) in comparison with ferrous sulphate supplemented milk (2 mg/100 kcal) in infants (6 to 12 months) with latent iron deficiency by measuring serum ferritin value after 2 months of consumption of studied milks.

NCT ID: NCT00548860 Completed - Anemia Clinical Trials

Safety of FCM vs. Standard of Care in Treating Iron Deficiency Anemia in Heavy Uterine Bleeding and Post Partum Patients

Start date: October 2007
Phase: Phase 3
Study type: Interventional

The Objective of this study is to study the safety of FCM in patients with anemia caused by Heavy Uterine Bleeding and the Post Partum state.

NCT ID: NCT00548691 Completed - Anemia Clinical Trials

Safety and Tolerability of FCM vs Standard of Care in Treating Iron Deficiency Anemia in Chronic Kidney Disease Patients

Start date: October 2007
Phase: Phase 3
Study type: Interventional

The Objective of this study is to study the safety of FCM in patients with anemia caused by chronic kidney failure

NCT ID: NCT00536666 Completed - Clinical trials for Chronic Kidney Disease

A Study of Iron Oligosaccharide in Chronic Kidney Disease Patients

Start date: May 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the safety profile of iron oligosaccharide in patients with chronic kidney disease with a need for parenteral iron.

NCT ID: NCT00535561 Completed - Clinical trials for Iron Deficiency Anemia

Iron Deficiency Anemia Can be an Indication for Treatment of Subclinical Hypothyroidism

Start date: June 2007
Phase: Phase 1
Study type: Interventional

To determine whether iron deficiency anemia can be an indication for the treatment of subclinical hypothyroidism.

NCT ID: NCT00534144 Completed - Clinical trials for Kidney Failure, Chronic

Comparison Between Effects of Two Iron Preparations on Protein in the Urine

Start date: September 2007
Phase: Phase 1
Study type: Interventional

This study will compare the effects of sodium ferric gluconate complex and iron sucrose on urine concentrations of various chemicals including protein

NCT ID: NCT00530374 Completed - Malnutrition Clinical Trials

Impact of Sprinkles on Infectious Morbidity When Moderate to Severe Pediatric Malnutrition Is Highly Prevalent

Start date: November 2007
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the safety profile of oral iron supplementation (OIS) with Sprinkles in a pediatric population with high prevalence of Iron deficiency (ID) and moderate or severe malnutrition (MSM); the efficacy profile will also be investigated.

NCT ID: NCT00520780 Completed - Clinical trials for Chronic Heart Failure

Ferinject® Assessment in Patients With Iron Deficiency and Chronic Heart Failure (FAIR-HF)

FAIR-HF
Start date: April 2007
Phase: Phase 3
Study type: Interventional

This study is designed to evaluate the efficacy of Ferinject® in improving symptoms of CHF in patients with iron deficiency. Analyses will focus both on subjective and objective measures. Furthermore, the tolerability and safety of Ferinject® treatment will be evaluated.