Iron deficiency anemia is the most common nutritional deficiency worldwide, occurring when the body lacks enough iron to produce adequate hemoglobin, leading to fatigue, weakness, reduced exercise tolerance, and impaired cognitive function. Underlying causes range from poor dietary intake to chronic blood loss, and treatment must address both the deficiency and its source.
What's actually going on in research
Intravenous iron formulations have become increasingly favored over oral iron for patients with absorption issues or intolerance, and several newer IV iron preparations allow faster infusion and single-dose repletion. Trials are comparing oral and IV approaches across various patient populations, studying the optimal timing of iron therapy in heart failure and chronic kidney disease, and investigating whether correcting iron deficiency independent of hemoglobin levels improves outcomes.
IV iron in heart failure
Ferric carboxymaltose and other IV iron formulations are being tested in patients with heart failure and iron deficiency to determine whether iron repletion reduces hospitalizations and improves exercise capacity.
Oral iron tolerability
Novel oral iron formulations with reduced gastrointestinal side effects are in trials, aiming to improve adherence in patients who cannot receive or access intravenous therapy.
Iron in chronic kidney disease
The optimal iron repletion target and formulation in patients with chronic kidney disease — who lose iron through dialysis and have impaired absorption — are being refined in ongoing trials.
What to know before you search
Eligibility depends on hemoglobin level, ferritin and transferrin saturation, underlying cause, and whether oral iron has already been tried.
What types of trials are currently open
- IV iron formulation trials — Comparing newer intravenous iron preparations for speed, safety, and degree of iron repletion.
- Oral iron trials — Testing formulations and dosing schedules that maximize absorption while reducing gastrointestinal side effects.
- Heart failure trials — Evaluating whether iron therapy improves exercise capacity and reduces hospitalizations in iron-deficient heart failure.
- Chronic kidney disease trials — Studying iron repletion strategies in patients on dialysis or with advanced kidney disease.
- Pediatric trials — Testing iron supplementation strategies in children and adolescents with deficiency anemia.
Recently added Iron Deficiency Anemia trials
FACE-APPS-Based Approach for Improving Iron Deficiency Anaemia Indicators Among Female Adolescents at Marginalized Communities
This study aims to evaluate the effect of the Face-to-face Assisted Counselling with Enhanced Application School-Based Approach (FACE-APPS-Based Approach) on anemia indicators among female adolescents. The study is a prospective, randomized controlled trial. A total of 160 female adolescents with hemoglobin levels below 12.0 g/dL will be recruited from 7 secondary schools. Random assignment at the individual level, stratified by baseline anemia status, will be used to ensure balance. For participants in the intervention group, the intervention will be designed by an interdisciplinary team and administered over 4 months, comprising 8 face-to-face counseling sessions and 8 parallel mobile application modules. Control group participants will receive standard care (diagnosis and referral). The primary outcomes are the mean differences in hemoglobin and serum ferritin levels. Secondary outcomes are engagement among female adolescents (attendance at counseling sessions and completion of mobile application modules).
Acupoint TENS vs Resistance Training for Iron Deficiency Anemia
The current study is designed to compare between the effect of transcutaneous electrical acupoint stimulation and resistance exercises on hemoglobin level in women with iron deficiency anemia.The design of this study will be a randomized controlled trial (RCT) pretest post-test assessment.Sixty women diagnosed with iron deficiency anemia will be recruited in this study from Kafrelshiekh University Hospital, Kafrelshiekh Governorate, Egypt. Their ages will be ranged from 20 to 30 years old, and they will be randomly divided into three equal (n= 20) groups. Change in hemoglobin concentration (g/dL) after the intervention period and changes in RBC count, MCV, MCH, RDW, serum ferritin, fatigue level, and functional exercise capacity after treatment will be measured.
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