Clinical Trial

Treatment of Anaemia After Caesarean With Intravenous Versus Oral Iron and Postpartum Depression

Study acronym: IRON-DEP
Recruiting Phase 4
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Summary
The objectif of the IRON-DEP Study is to assess the efficacy of intravenous (IV) versus oral iron treatment on the prevalence of postpartum depression (PPD) in women with moderate iron deficiency anemia after caesarean delivery.
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2025-02-13; most recent amendment 2026-06-19.
Status change: Not Yet Recruiting → Recruiting 2026-05-29
Trial Details
NCT Number NCT06833788
Lead Sponsor Assistance Publique - Hôpitaux de Paris
Conditions Postpartum Depression (PPD)
Enrollment 2,860 participants
Start Date 2025-10-22
Primary Completion 2028-06-22 (estimated)
Study Completion 2028-10-30 (estimated)
Updated on ClinicalTrials.gov 2026-06-23