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NCT07303595 · ClinicalTrials.gov registry record · NA
Mom Multi Postnatal Supplementation Trial
A NA study of Postnatal Care, sponsored by Perelel.
- Recruiting
- Registry status
- NA
- Development phase
- 80
- Enrollment target
- 1
- Study location
NCT07303595 is a NA study of Postnatal Care that is actively recruiting participants, run by Perelel. The registered enrollment target is 80 participants. The trial reports 1 study location across 1 state.
The verdict
NCT07303595, a NA study of Postnatal Care, is actively recruiting participants, sponsored by Perelel.
- RECRUITING
- Registry status
- NA
- Development phase
- 80 participants
- Enrollment target
- 1
- Study location
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
Conditions Studied
Interventions
- DIETARY_SUPPLEMENT Placebo
- DIETARY_SUPPLEMENT Perelel Mom Multi
Study Locations (1)
Georgia
- UGA Clinical & Translational Unit - Athens
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2025-11-10 |
| Est. Completion | 2026-10 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT07303595
The ClinicalTrials.gov registry entry for NCT07303595 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Perelel, which has 3 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Postnatal Care appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.
NCT07303595 reports 1 study location spanning 1 distinct geographic area - top geographies include Georgia.
Frequently Asked Questions
What is clinical trial NCT07303595 about?
NCT07303595 is a clinical study titled "Mom Multi Postnatal Supplementation Trial". 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-...
What is the current status of trial NCT07303595?
This trial is currently recruiting. It is a NA study. The enrollment target is 80 participants. The study started on 2025-11-10. Estimated completion is 2026-10.
What conditions does trial NCT07303595 study?
This clinical trial studies the following conditions: Postnatal Care.
What interventions are being tested in trial NCT07303595?
The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Perelel Mom Multi (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT07303595?
This trial is sponsored by Perelel, which has 3 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07303595 being conducted?
This trial has 1 study location across Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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