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Study identifier: NCT06833788 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Postpartum Depression (PPD)  ·  Sponsor: Assistance Publique - Hôpitaux de Paris

PhasePhase 4
Planned participants2860
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Marie-Pierre BONNET, MD, PhD  ·  (+) 33 1 71 73 89 56  ·  marie-pierre.bonnet@aphp.fr

Sarra POCHON, MD  ·  0033 1 42 16 75 74  ·  sarra.pochon@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (1)

CHU Armand -Trousseau, AP-HP Service d'anesthésie-réanimation chirurgicaleParis, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06833788