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Recruiting NCT06833788

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

Phase IV Interventional Postpartum Depression (PPD)

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Ferric carboxymaltose IV, TIMOFÉROL®.
Who it may be relevant to
Registry conditions: Postpartum Depression (PPD). Basic parameters: from 18 years · Female.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
France
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Treatment of Anaemia After Caesarean With Intravenous Versus Oral Iron and Postpartum Depression: a Multicentric Randomized Open-labelled Controlled Trial

Overview

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.

Detailed description

PPD is a frequent (10-20% of delivery) and serious condition that has a detrimental impact on both maternal and child health by altering the quality of their interactions. Moreover, it is a significant risk factor for suicide, which is the leading cause of maternal death.

The increased risk of PPD in women with postpartum anemia has been documented. Women who delivered by cesarean are particularly vulnerable to this risk as this mode of delivery is a risk factor for both postpartum anaemia and postpartum depression. Therefore, correcting anemia and preventing PPD in this population represent a major public health priority.

First line treatment recommended for iron deficiency moderate anaemia (8.0g/dL≤ Hb ≤10.0g/dL) is oral iron. However oral iron is associated with very frequent adverse effects, contributing to poor tolerance and compliance of this treatment. Actually, IV iron is indicated in women with non-severe postpartum anaemia with lack of response or intolerance to oral iron treatment. There is growing interest in the use of intravenous iron and several randomized controlled trials demonstrated that IV iron is significantly more efficient than oral iron supplementation to correct moderate postpartum anaemia and increase haemoglobin level. However, none of them compared the efficacy of IV iron versus oral iron on postpartum depression as a primary outcome.

The hypothesis of the IRON-DEP Study is that, among women with moderate postpartum iron deficiency anaemia after caesarean delivery, the prevalence of PPD symptoms at 8 weeks after delivery is lower in women treated with IV iron than in those treated with oral iron.

The IRON-DEP trial is a phase IV national multicenter comparative randomized controlled superiority open-label trial with 2 parallel groups.

Implementation of the study :

* 24 french maternity units will be participating * Women who delivered by cesarean admitted in the postpartum maternity ward, with postpartum anaemia will be screened to check the inclusion and exclusion criteria. * The investigator will inform the eligible patient about the protocol and obtain the written consent * The randomization will take place during the hospitalization for caesarean delivery and will be stratified on the centre and on the initial severity of post-partum anemia (according to the postpartum hemoglobin level). * IV iron will be administered during hospitalization and participants in the oral iron group will start their treatment during their hospitalization for 8 weeks treatment. * A follow up visit at 8 weeks postpartum will be planned at the maternity unit for all participants * All participants will fill in self-assessment questionnaires (online or paper form) at inclusion, 8 weeks and 6 months postpartum follow up.

Interventions

  • Drug Ferric carboxymaltose IV
    Single dose of Ferric carboxymaltose 1000 mg (20mL) IV infusion (20ml vial of 1000mg iron or two 10ml vials of 500mg)
  • Drug TIMOFÉROL®
    100 mg once a day (2 pills of TIMOFÉROL® 50mg)

Primary outcome measures

  • Prevalence of PostPartum Depression (PPD) symptoms defined by an Edinburg Postpartum Depression Scale (EPDS) score ≥ 11 [Time frame: 8 weeks postpartum]
Secondary outcome measures (12)
  • The mean Haemoglobin (Hb) level [Time frame: 8 weeks postpartum]
  • Change in postpartum Haemoglobin (Hb) level [Time frame: At Inclusion and at 8 weeks postpartum]
  • The proportion of women with Haemoglobin level < 12.0 g/dL [Time frame: 8 weeks postpartum]
  • The mean ferritinemia level [Time frame: At Inclusion and at 8 weeks postpartum]
  • The mean change in ferritinemia level [Time frame: At Inclusion and at 8 weeks postpartum]
  • The proportion of women with ferritinemia < 20 ng/mL [Time frame: 8 weeks postpartum]
  • Mean EPDS score [Time frame: 8 weeks postpartum, 6 months postpartum]
  • The proportions of participants with moderate depressive symptoms level defined by an EPDS ≥ 11 and <13 [Time frame: 8 weeks postpartum, 6 months postpartum]
  • The proportions of participants with high depressive symptoms level defined by an EPDS ≥13 [Time frame: 8 weeks postpartum, 6 months postpartum]
  • The mean change in EPDS score [Time frame: 8 weeks postpartum, 6 months postpartum]
  • The need for red blood cell transfusion [Time frame: From discharge to 8 weeks postpartum]
  • The mean fatigue score measured by the Multidimensional Fatigue Inventory score-20 (MFI-20) [Time frame: 8 weeks postpartum, 6 months postpartum]

Eligibility criteria

Pre-inclusion criteria:

  • Age ≥18 years
  • Caesarean delivery (elective or in emergency)
  • Gestational age at delivery ≥ 32 weeks
  • 8.0 g/dL ≤ postoperative Hb level ≤ 10.0 g/dL measured within 72 hours postpartum
  • Informed consent form signed
  • Hospitalization in the postpartum maternity ward
  • National social security coverage including AME

Inclusion criteria

  • Ferritinemia ≤ 100 ng/mL OR transferrin saturation ≤ 20% measured after postoperative Hb level measurement
  • EPDS score in the immediate postpartum <11 with a "never" answer to question n°10

Exclusion criteria

  • Stillbirth or neonatal death
  • Last body weight available before inclusion (measured at the end of pregnancy or in postpartum) < 35kg or > 100kg
  • Biermer disease
  • Hemochromatosis
  • Homozygous sickle cell disease or thalassemia
  • Chronic iron supplementation (outside pregnancy)
  • Known hypersensitivity or allergy to the studied drugs (IV or oral iron)
  • Contra-indication to the studied drugs (IV or oral iron)
  • Severe asthma (with daily background treatment)
  • Any known severe renal or liver disorder
  • Active acute infection
  • Diagnosis of schizophrenia or physical and intellectual state incompatible with a reliable self-evaluation
  • Women currently treated with medication or with Electro Convulsion Therapy (ECT) for depression or bipolar disorders
  • Participation in another clinical trial involving an intervention with the following risks:
  • A change (increase or decrease in value) in Haemoglobin measured at 2 months postpartum OR
  • A change in EPDS score measured at 2 and 6 months postpartum OR
  • A trial exploring an intervention with a specific anaphylactic risk (reported as a potential adverse events in the protocol of the other trial) administered during the postpartum hospitalization period.
  • Poor understanding of the French language
  • Legal protection (curatorship or tutorship)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Health services research

Study locations

France · 1 center
  • CHU Armand -Trousseau, AP-HP Service d'anesthésie-réanimation chirurgicale — Paris

Identifiers

NCT: NCT06833788 · APHP220806 · 2023-503283-17-00

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗