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Mom Multi Postnatal Supplementation Trial

Perelel Inc. · with University of Georgia · NCT07303595

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Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

Compensation
Not posted. Ask the study team before screening.
Who can join
Ages 18+ · Women only
Healthy volunteers
Not accepted (a condition is required)
Study type
Interventional · Not applicable
Target enrollment
80
US sites recruiting
1
Study start
November 10, 2025
Record last updated
December 26, 2025

Status re-checked against ClinicalTrials.gov within the last 12 hours.

What the study 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

Being studied: Perelel Mom Multi; Placebo

Conditions: Postnatal Care

Eligibility criteria

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion criteria

  • Healthy, postpartum women (\~4 weeks [± 2 weeks]) with infants born term and singleton
  • Not pregnant during the study period
  • Able to understand (written and spoken) English or Spanish.

Exclusion criteria

  • Cardiometabolic disease
  • Past pregnancy complications (gestational diabetes, hypertension)
  • malabsorption syndromes (IBS, IBD, Crohn's, Colitis, Celiac)
  • Caily use of medications which may affect nutrient absorption
  • chronic alcohol use (> 4 alcoholic drinks/day)
  • those prescribed postnatal MVM supplements by their physician
  • unwilling to discontinue dietary supplementation containing any of the active components in the study product over the study period
  • Women should not have an allergy or intolerance to active or inactive product ingredients.

Recruiting US locations

  • UGA Clinical & Translational Unit

    Athens, GA 30606

    Site contact: Sina Gallo, PHD · 706-713-2721 · ctru@uga.edu

Study contacts (from the official record)

  • Sina Gallo, PhD, MSc, RD · 706-542-4847 · ctru@uga.edu
Mom Multi Postnatal Supplementation Trial (NCT07303595) | Bored Studies