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Anemia, Iron Deficiency clinical trials

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NCT ID: NCT03365570 Completed - Clinical trials for Iron Deficiency Anemia

Prevalence of Oral Manifestations of Iron Deficiency Anemia in a Sample of Egyptian Population

Start date: May 1, 2018
Phase:
Study type: Observational

According to WHO Reportin 2002, iron deficiency anemia was considered to be the most important contributing factor to the global burden of anemia. Children and women in reproductive ages are more at risk factor for developing iron deficiency anemia.No previous study has been held to assess prevalence of oral manifestations of iron deficiency anemia as a hospital-based cross-sectional study on a sample of Egyptian patients in hematology department (no previous data recorded).

NCT ID: NCT03359447 Recruiting - Anemia Clinical Trials

Iron Deficiency Anemia, Iron Supplementation and Genomic Stability in Infants

Start date: August 1, 2017
Phase: Phase 4
Study type: Interventional

This study compares weekly versus daily administration of iron for prevention of anemia in 6 months old infants. One third of the infants that are exclusively breast fed will not receive iron, the second third will receive iron weekly and the last third will receive iron daily. Half of the infants that take infant formula will receive iron weekly and the other half will receive iron daily.

NCT ID: NCT03357510 Completed - Iron-deficiency Clinical Trials

The Effect of the Prebiotic Galacto-oligosaccharide on Iron Absorption With Micronutrient Powders in Kenyan Infants

Start date: April 16, 2018
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether single doses of the prebiotic galacto-oligosaccharide (GOS) added to iron-fortified meals with micronutrient powders increase iron absorption compared to a 3 weeks pre-feeding of GOS.

NCT ID: NCT03355287 Not yet recruiting - Clinical trials for Iron Deficiency Anemia

Iron Status in Infants in Ethiopia.

Start date: November 2018
Phase: N/A
Study type: Interventional

To assess the impact of soil iron intake from teff flour on iron status in infants in Debre Zeit, Ethiopia.

NCT ID: NCT03353662 Not yet recruiting - Iron-deficiency Clinical Trials

Sub Regional Micronutrient Survey in Ethiopia

Start date: September 2018
Phase:
Study type: Observational

To conduct a sub-regional micronutrient survey (SRMNS) assessing the prevalence of vitamin A, Zn, and Fe status in the country

NCT ID: NCT03347513 Recruiting - Clinical trials for Pregnancy Complications

Eradication of H-pylori in Pregnancy and Its Effect on Iron Replacement Therapy?

Start date: November 25, 2017
Phase: Phase 4
Study type: Interventional

the effect of eradication of H-pylori in pregnant patients with iron deficiency anemia on the level of hemoglobin after iron therapy.

NCT ID: NCT03346213 Completed - Anemia Clinical Trials

CArdio PulmOnary Exercise Testing and IntRAvenous Iron- 'CAPOEIRA-I STUDY'

CAPOEIRA-I
Start date: February 2, 2018
Phase:
Study type: Observational

Red blood cells contain a chemical called haemoglobin which carries oxygen from the lungs around the body. When the amount of haemoglobin is reduced, a patient is 'anaemic'. Anaemia can have many causes, but affects about a third of patients having major surgery in hospital. After their operation these anaemic patients are more likely to suffer serious complications. This may be because the body needs extra oxygen - and so enough haemoglobin - to heal and recover successfully from the trauma of surgery. For a similar reason, patients' overall fitness before surgery is very important. Less fit patients are much more likely to get complications after surgery. To help us assess the risk of complications, the investigators measure patients' fitness before surgery using a cycling exercise test. The investigators monitor a number of things that show us how well the heart, the lungs and the muscles respond when they are under stress. People who are very anaemic tend to perform less well on this cycling test. Anaemia is often due to a lack of iron, which helps make haemoglobin. Usually people get iron from foods such as red meat and spinach. Some conditions mean that patients lose iron, such as a tumour bleeding. Other illnesses make it difficult for the body to absorb iron from the gut in the first place. Both lead to a state of low iron in the body and eventually this leads to anaemia. One way to treat anaemia quickly before surgery is to give iron into the bloodstream (intra-venous). It is thought that this might reduce the risk of complications after surgery, but it is not known whether this is because it improves overall fitness, or for other reasons. The investigators plan to carry out a study called CAPOEIRA-I (CArdio PulmOnary Exercise testing and IntRAvenous Iron) to find out whether giving patients intravenous iron improves their fitness. The investigators will measure this by doing a cycle exercise test before and then at least 10 days after the iron is given. The investigators will also measure how much the total amount of haemoglobin chnages with iron treatment. Intravenous iron is already routinely used for these patients, so the only additional activity for the study is the extra exercise test, some extra blood tests and the measurement of haemoglobin after the iron has taken effect.

NCT ID: NCT03344523 Not yet recruiting - Clinical trials for Chronic Heart Failure

Evaluating Iron Protein Succinylate Oral Solution in Treating Chronic Heart Failure and Iron Deficiency

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

This study aims to evaluate the effect of standard heart failure therapy plus oral solution with protein succinylate iron compared to placebo on the primary end point of 6 minute walk distance at 24th week in patients with chronic ejection fraction reduction heart failure and iron deficiency.

NCT ID: NCT03332602 Completed - Iron-deficiency Clinical Trials

Iron Absorption From Encapsulated Iron Sulphate in Microspheres

Start date: April 4, 2018
Phase: N/A
Study type: Interventional

Food fortification has shown to be efficacious to alleviate the burden of micronutrient deficiencies. Ensuring the bioavailability of iron and maintaining the sensory quality and stability of the fortified food and other added micronutrients remains a challenge. Soluble iron compounds cause minor organoleptic changes in foods but their bioavailability in man is rather low. Water-soluble iron compounds, such as ferrous sulphate (FeSO4), are the compounds in which the iron is most bioavailable; however, they often cause unfavorable sensory changes. Encapsulation of iron has excellent potential for overcoming unwanted sensory changes and iodine losses in salt, while maintaining acceptable bioavailability. In the present project, we would like to investigate the iron bioavailability from a new formulation of encapsulated iron sulphate based on hyaluronic acid (HA) and a polymer from the eudragit family.

NCT ID: NCT03325270 Completed - Iron-deficiency Clinical Trials

Effect of Prebiotics on Iron Absorption in Women With Low Iron Stores

Fe_GOS_1
Start date: January 10, 2018
Phase: N/A
Study type: Interventional

Rationale: According to the WHO, iron deficiency is still the most common and widespread nutritional disorder in the world. Current iron supplements have limitations in terms of bioavailability and tolerability. Prebiotic fibers, such as galacto-oligosaccharides (GOS), selectively enhance growth of beneficial colonic bacteria. Prebiotics in general enhance the production of short-chain fatty acids (SCFAs) and thereby decrease luminal pH. Through the reduction in colonic pH, prebiotics can enhance absorption of minerals such as calcium and magnesium and they have been proposed to potentially improve iron absorption as well. The primary objective of this study is to investigate the effect of an addition of GOS to an iron supplement on iron absorption in iron deplete, healthy, normal weight women.