Actively Recruiting

Phase Not Applicable
Age: 18Years +
FEMALE
NCT07303595

Mom Multi Postnatal Supplementation Trial

Led by Perelel Inc. · Updated on 2025-12-26

80

Participants Needed

1

Research Sites

46 weeks

Total Duration

On this page

Sponsors

P

Perelel Inc.

Lead Sponsor

U

University of Georgia

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this clinical trial is to learn if a vitamin and mineral supplement designed specifically for women after childbirth can improve their nutrition and health in women who are pregnant or have recently given birth (within 6 weeks). The main question it aims to answer is: Can a postpartum-specific vitamin and mineral supplement help improve nutritional status and health outcomes in women after giving birth? Researchers will compare women who take the new postpartum vitamin and mineral supplement to women who take a placebo (fake pills without active ingredients) to see if the supplement improves their nutritional health. Participants will: Attend 2 visits at University of Georgia (1-1.5 hours each) over 12 weeks Participate in 2 phone calls between visits Stop taking other vitamin/mineral supplements during the study Have blood drawn to test vitamin and mineral levels Provide urine samples and breastmilk samples if breastfeeding (optional) Have height, weight, and skin color measured Complete questionnaires about health, pregnancy, and mental wellness Answer questions about daily food and drink intake Take either the study supplement or placebo daily

CONDITIONS

Official Title

Mom Multi Postnatal Supplementation Trial

Who Can Participate

Age: 18Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

  • Healthy, postpartum women approximately 4 weeks postpartum (± 2 weeks) with a term, singleton infant
  • Not pregnant during the study period
  • Able to understand written and spoken English or Spanish
Not Eligible

You will not qualify if you...

  • History of cardiometabolic disease
  • Past pregnancy complications such as gestational diabetes or hypertension
  • Malabsorption syndromes including IBS, IBD, Crohn's disease, colitis, or celiac disease
  • Daily use of medications that may affect nutrient absorption
  • Chronic alcohol use of more than 4 alcoholic drinks per day
  • Currently prescribed postnatal multivitamin-mineral supplements by a physician
  • Unwillingness to stop other dietary supplements containing active study product ingredients during the study
  • Allergy or intolerance to any active or inactive ingredients in the study product

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

UGA Clinical & Translational Unit

Athens, Georgia, United States, 30606

Actively Recruiting

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Research Team

S

Sina Gallo, PhD, MSc, RD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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