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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
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