Clin2
NCT06833788Possibly a fitRecruiting

IV vs. oral iron for anemia after c-section and depression risk

Postpartum Depression (PPD)

Treatments studied

Part of Mental health, Women’s health & pregnancy clinical trials.

This trial compares intravenous (IV) iron with oral iron pills to treat anemia after a C-section, and looks at whether iron treatment affects the risk of postpartum depression. You may be eligible if you had a C-section, are at least 18, delivered at 32 weeks or later, have mild to moderate anemia, and low iron stores.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 4
Enrollment
2,860 people
Ages
18 years and older
Study type
Interventional

Who can take part

  • You are 18 years or older
  • You delivered your baby by C-section (planned or emergency)
  • You were at least 32 weeks pregnant when you delivered
  • Your hemoglobin (red blood cell level) is between 8.0 and 10.0 g/dL within 3 days after delivery
  • Your iron level is low (ferritin 100 or less, or transferrin saturation 20% or less)
  • You have a low score on a depression screening questionnaire (EPDS below 11, and you answered 'never' to the last question)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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