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

Study acronym: IRON-DEP
StatusRecruiting
PhasePhase 4
Started2025-10-22
View on ClinicalTrials.gov ↗

Amendment history

2026-06-19
Study Status v3
Re-verified, no change to tracked fields
2026-05-29
Not Yet Recruiting→Recruiting Study Status, Oversight, Eligibility, Contacts/Locations v2
Trial statusNot Yet Recruiting→Recruiting
Primary completion date2028-06→2028-06-22
Completion date2028-10→2028-10-30
Start dateestimated 2025-09→confirmed 2025-10-22
Eligibility criteria+60 characters
[...] stion n°10 Exclusion Criteria: Stillbirth or neonatal death BodyLast body weight available before inclusion (measured at the end of pregnancy or in postpartum) < 35kg or > 100kg at the end of pregnancy Biermer disease Hemochromatosis Homozygous sickle cell dise [...]
Study sitesdetails revised at 1 of 1 site
2025-08-06
Study Identification, Study Status, Arms and Interventions v1
Completion date2028-12→2028-10
Start date2025-04→2025-09
Study titlerevised
Treatment of Anaemia After Caesarean withWith Intravenous Versus Oral Iron and Postpartum Depression
2025-02-13
Original filing
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.
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 2026-09-21