New treatment option for Postnatal Care
Official title Mom Multi Postnatal Supplementation Trial
ClinicalTrials.gov ID: NCT07303595
What this study is testing
- What it's testing
- 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?
- Time commitment: about 12 weeks
- You might receive a placebo (an inactive treatment) instead of the study drug.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older, women only
You may be able to join if
- 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.
You likely can't join if
- 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
See the full eligibility 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.
- 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.
The study team makes the final eligibility decision.
Where it's taking place
- Athens, Georgia, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The study runs about 12 weeks per participant, based on its public description. The team confirms the exact schedule and number of visits before you enroll.
Who can join this trial?
This study is enrolling female, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Athens, Georgia, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.