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Clinical Trials in the USA / NCT07303595
Recruiting Not applicable

Mom Multi Postnatal Supplementation Trial

NCT07303595 · tracked via the Priya Life Science USA tracker
Sponsor
Perelel Inc.
Phase
Not applicable
Started
2025-11-10
Last updated
2025-12-26

Condition(s) studied

Postnatal Care

Investigational drug(s) / intervention(s)

Perelel Mom MultiPlacebo

Perelel Mom Multi: Daily Perelel postnatal multivitamin supplement throughout intervention

Placebo: Daily placebo capsules throughout intervention

Study summary

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

Eligibility

Sex
FEMALE
Min age
18 Years
Max age
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
UGA Clinical & Translational Unit Athens Georgia Recruiting

More Perelel Inc. trials in the USA

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07303595 on ClinicalTrials.gov ↗ ← All trials in the USA