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Multiple Micronutrient Supplementation (MMS) Iron Dose Acceptability Crossover Trial

Multiple Micronutrient Supplementation (MMS) Iron Dose Acceptability Crossover Trial

Recruiting
18 years and older
Female
Phase 3
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  • Simplified (AI rewritten)

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Overview

This is an individually randomized cross-over trial to assess acceptability, preference, and perceived side effects of MMS formulations with 30 mg, 45 mg and 60 mg of iron.

Eligibility

Inclusion Criteria:

  • Attending first ANC visit at the study clinic
  • Pregnant women ≤ 15 weeks of gestation
  • Aged ≥ 18 years
  • Intending to stay in Dar es Salaam for the duration of study
  • Provides informed consent

Exclusion Criteria:

  • Severe anemia (defined as Hb <8.5 g/dL per Tanzania standard of care)
  • Sickle cell disease (SS,SC, CC genotype) as tested by HemoTypeSC
  • Concurrent participation in other nutritional supplementation trial
  • Pregnant women with disability or condition which would impair their ability to provide informed consent and complete study procedures.

Study details
    Pregnancy Related

NCT06069869

George Washington University

15 October 2025

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