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Iron Deficiency Anemia clinical trials

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NCT ID: NCT04131608 Not yet recruiting - Clinical trials for Iron Deficiency Anemia

Effect of Iron Deficiency Anemia on HBA1C in Patients With Diabetic Foot Ulcer Grade (1and2)

Start date: February 1, 2021
Phase:
Study type: Observational

Diabetic foot ulcer is the commonest cause of severe limb ischemia in diabetes mellitus And development of anemia is an additional burden to the microvascular complications of diabetes

NCT ID: NCT04130828 Completed - Clinical trials for Iron Deficiency Anemia

Thrice-weekly Versus Thrice-daily Oral Ferrous Fumarate Treatment in Adult Patients With Iron Deficiency Anemia

Start date: January 21, 2020
Phase: Phase 3
Study type: Interventional

Iron deficiency anemia is a global health problem and the most common cause of anemia worldwide. Patients with iron deficiency and Iron deficiency anemia can present with a multitude of symptoms including fatigue, dyspnea on exertion, dysphagia, pallor, palpitations, headaches, tinnitus, taste disturbance and pica. Oral iron supplementation is associated with increasing hemoglobin in multiple studies in women, pregnant women and elderly patients. However, the optimal dose and frequency of oral iron supplementation for treatment remains unclear. The current proposed study attempts to address this gap in the literature.

NCT ID: NCT04087993 Suspended - Clinical trials for Iron Deficiency Anemia

Polyglucoferron Compared to i.v. Ferric Carboxymaltose and Oral Iron Substitution in Preoperative Treatment of Iron Deficiency Anaemia in Patients

IDA-I
Start date: May 15, 2020
Phase: Phase 3
Study type: Interventional

Patients with IDA and for whom fast replenishment of iron stores is necessary, e.g. if its not appropriated to postpone surgery, will be identified within 28 to 42 days before surgery. Patients will be randomised to receive either Polyglucoferron intravenously (i.v.), Ferric Carboxymaltose i.v. or oral iron substitution with Ferrous sulfate.

NCT ID: NCT04079322 Completed - Clinical trials for Iron Deficiency Anemia

Iron Absorption and Exercise

Start date: August 22, 2019
Phase: N/A
Study type: Interventional

Iron is a nutritionally essential mineral required for optimal physical and cognitive performance. Endurance exercise often leads to declines in iron status; however, the reason for the decline is not known. The primary objective of the proposed study is to determine the effects of an acute bout of strenuous endurance exercise on iron absorption and status and markers of inflammation in human volunteers. The investigators hypothesize that an acute bout of strenuous endurance exercise, compared to rest, will reduce iron absorption, resulting in diminished iron status, and that reduced iron absorption will be negatively associated with markers of inflammation. A secondary objective is to monitor iron status throughout a season of competition.

NCT ID: NCT04018300 Completed - Clinical trials for Iron Deficiency Anemia

Iron Supplementation and Side Effects

Start date: January 8, 2018
Phase: N/A
Study type: Interventional

The objective of this study is to examine patient-reported gastrointestinal side effects, as well as iron status indicators, inflammatory markers and oxidative stress following administration of ferrous sulfate and iron-enriched Aspergillus oryzae supplementation.

NCT ID: NCT03944733 Withdrawn - Clinical trials for Iron Deficiency Anemia

Iron Status, Maternal Depressive Symptoms, and Mother-child Interactions

IDinteract
Start date: December 1, 2019
Phase: N/A
Study type: Interventional

This study aims to examine the relation between iron status and maternal-child interactions as well as maternal depressive symptoms in mothers from central Pennsylvania.

NCT ID: NCT03940430 Completed - Clinical trials for Iron Deficiency Anemia

Lactoferrin Versus Ferrous Sulfate in Management of Iron Deficiency Anemia Among Female Medical Ain Shams Students

Start date: September 10, 2018
Phase: Phase 2/Phase 3
Study type: Interventional

This study aims to compare the efficacy of lactoferrin versus iron supplementation versus two combined supplementation on iron deficiency anemia in female medical Ain Shams students by using iron profile.

NCT ID: NCT03933813 Terminated - Anemia Clinical Trials

Evaluation and Treatment of Iron Deficiency in Ovarian Cancer Patients

Start date: July 29, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

This study tests the hypothesis that IV iron sucrose infusions given to iron deficient ovarian cancer patients prior to debulking surgery can improve pre-operative iron stores and decrease transfusion of packed red blood cells in the peri-operative period. 21 participants at least 18 years of age with epithelial ovarian cancer of any stage requiring neoadjuvant chemotherapy and surgery will be enrolled. Participants will be on study for a period of up to 3 months.

NCT ID: NCT03915327 Not yet recruiting - Clinical trials for Iron Deficiency Anemia

Short-term Intravenous Iron Isomaltose Anhydride for IDA

Start date: July 5, 2024
Phase: N/A
Study type: Interventional

This prospective, randomized, controlled study aims to evaluate the impact of short-term intravenous iron isomaltose anhydride on postoperative recovery and the requirement for allogeneic red blood cells (RBC) transfusion in preoperative Iron-deficiency anemia (IDA) patients receiving orthopedic surgery, thus facilitating developing a simple and effective iron supplement approach for patients' recovery.

NCT ID: NCT03897673 Enrolling by invitation - Anemia Clinical Trials

Optimizing Benefits While Reducing Risks of Iron in Malaria-endemic Areas

OptiM
Start date: September 1, 2019
Phase: N/A
Study type: Interventional

Daily iron (ferrous sulfate, 2 mg/kg/day) or placebo syrup for first four months (112 days) of the 12-month (336-day) study. Children in the immediate iron group will receive iron syrup for the first three months (84 days) and placebo syrup for the fourth month. Children in the delayed iron group will receive placebo syrup for the first month (28 days) and iron syrup for the second, third, and fourth months.