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Search / Trial NCT06069856

Multiple Micronutrient Supplementation (MMS) vs IFA Acceptability Crossover Trial

Launched by GEORGE WASHINGTON UNIVERSITY · Sep 29, 2023

Trial Information

Current as of June 26, 2025

Not yet recruiting

Keywords

Acceptability Multiple Micronutrient Supplementation Iron Ifa Tanzania

ClinConnect Summary

This clinical trial is looking at how pregnant women feel about two different types of supplements: one that contains iron and is called Iron Folic Acid (IFA) and another that has multiple vitamins and minerals, also with iron, called Multiple Micronutrient Supplementation (MMS). The researchers want to see which supplement women prefer, how they feel about taking them, and if they experience any side effects. This study is important because good nutrition during pregnancy is crucial for the health of both the mother and the baby.

To participate in this trial, you need to be a pregnant woman who is less than 15 weeks along, at least 18 years old, and able to stay in the study area for the entire duration of the trial. You should also be attending your first antenatal care visit at the study clinic and provide informed consent to join. However, if you have severe anemia, certain genetic blood disorders, or are already in another nutrition study, you won’t be able to take part. If you do join, you can expect to try both types of supplements during the study and share your thoughts on them. This information will help improve nutrition support for pregnant women in the future.

Gender

FEMALE

Eligibility criteria

  • Inclusion Criteria:
  • Attending first ANC visit at the study clinic
  • Pregnant women ≤ 15 weeks of gestation
  • Aged ≥ 18 years
  • Intending to stay in the study area 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.

About George Washington University

George Washington University (GWU) is a leading academic institution dedicated to advancing medical research and education. As a clinical trial sponsor, GWU leverages its extensive resources and expertise to facilitate innovative studies that aim to improve healthcare outcomes. The university's commitment to ethical research practices, collaboration with multidisciplinary teams, and engagement with diverse populations underscores its role in addressing critical health challenges. By fostering a rigorous scientific environment, GWU strives to translate research findings into effective clinical applications, ultimately enhancing patient care and contributing to the broader medical community.

Locations

Patients applied

0 patients applied

Trial Officials

Blair Wylie, MD, MPH

Principal Investigator

Columbia University

Honorati Masanja, PhD

Principal Investigator

Ifakara Health Institute

Alfa Muhihi, PhD

Principal Investigator

Africa Academy of Public Health

Andrea Pembe, MD, MMed, PhD, FCOG

Principal Investigator

Muhimbili University of Health and Allied Sciences

Emily R Smith, ScD, MPH

Principal Investigator

The George Washington University

Christopher R Sudfeld, ScD, ScM

Principal Investigator

Harvard University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported