Condition: Non-Anemic Iron Deficiency · Sponsor: Istanbul University - Cerrahpasa
This study investigates the risk of anemia development in women aged 18-55 years with non-anemic iron deficiency and evaluates the clinical effects of oral iron therapy. The study consists of a two-month nutritional intervention phase followed by a one-month oral iron treatment phase. Participants first receive dietary counseling aimed at increasing iron intake and absorption. After two months, changes in hematologic parameters and symptoms are evaluated. Women with persistent iron deficiency then receive daily oral ferrous sulfate (80 mg elemental iron) for one month. The study aims to identify early predictors of anemia progression and to assess the impact of dietary modification and oral iron therapy on symptoms and laboratory findings.
This description comes directly from the study's public registry record.
Osman Demir, MD · +90 532 291 4470 · osman.demir@iuc.edu.tr
Ayşen Fenercioğlu, Assoc Prof · +90 537 964 5751 · aysen.fenercioglu@iuc.edu.tr
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| Kagıthane No. 5 Family Health Center | Kâğıthane, Istanbul, Turkey (Türkiye) | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07263529