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Anemia, Iron Deficiency clinical trials

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NCT ID: NCT00655408 Completed - Anemia Clinical Trials

Iron-Deficiency Anemia in Infants in Two Weekly Programs

IDA
Start date: April 2003
Phase: N/A
Study type: Interventional

This work aims at establishing the effectiveness of weekly doses of ferrous sulfate administered by mothers compared with weekly supplements administered directly by healthcare professionals, to reducing anemia prevalence.

NCT ID: NCT00642863 Completed - Clinical trials for Iron Deficiency Anemia

Brain and Behavior Depending on Timing of Iron Deficiency in Human Infants

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

It is common in many populations that babies develop iron deficiency or iron deficiency anemia (that is, too few healthy red blood cells due to lack of iron). This is due to rapid growth in infancy combined with limited sources of iron in the infant diet. The amount of iron the baby receives across the placenta during pregnancy is another important factor. This study focuses on infants who are born with less than the usual amount of iron in their bodies. The purposes of the study are to assess effects of lower iron at birth on infant behavior and development and to determine if providing iron supplements to such infants beginning at 6 weeks fosters healthier development. Another part of the study will determine the effects of iron deficiency anemia at different times during infant development.

NCT ID: NCT00613717 Completed - Clinical trials for Iron Deficiency Anemia

Healthy Infant Development Project

Start date: November 2009
Phase: N/A
Study type: Interventional

The Healthy Infant Development Project will determine if providing micronutrient supplements to mothers during pregnancy and infants in the first 9 months fosters healthy behavior and development in babies.

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: 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