Actively Recruiting
Perelel Prenatal Supplements vs. Generic Prenatal Supplements and Health of Mother and Baby (SUPPORT)
Led by University of Pittsburgh · Updated on 2026-02-04
600
Participants Needed
1
Research Sites
72 weeks
Total Duration
On this page
Sponsors
U
University of Pittsburgh
Lead Sponsor
P
Perelel Inc.
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if using Perelel-brand prenatal supplements versus a generic prenatal supplement improves the health of the mother and fetus (unborn baby) during pregnancy. The main question it aims to answer is: • How does taking Perelel prenatal supplements versus generic prenatal supplements during pregnancy change the nutritional markers in blood samples? Participants will: * Take either Perelel or generic prenatal supplements daily throughout pregnancy * Visit UPMC Magee-Womens Hospital once every trimester of pregnancy for blood draws and answering questionnaires In an observational part of this study for different participants, researchers will use blood tests and questionnaires only once during the first trimester to compare pregnant women without food insecurity to those with food insecurity.
CONDITIONS
Official Title
Perelel Prenatal Supplements vs. Generic Prenatal Supplements and Health of Mother and Baby (SUPPORT)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Pregnant with only one baby
- Identify as having food insecurity
- Receiving care at a Magee-Womens Hospital associated prenatal practice
- Less than 12 weeks' of pregnancy
You will not qualify if you...
- Currently using prenatal supplement(s)
- Unborn baby (fetus) identified as having a chromosomal or structural defect
- Have a condition that prevents absorption of nutrients from food
- History of medically treated thyroid disorder
- Ongoing steroid use
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
UPMC Magee-Womens Hospital
Pittsburgh, Pennsylvania, United States, 15213
Actively Recruiting
Research Team
J
Jeanette Boyce, RNC, MSN
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
SUPPORTIVE_CARE
Number of Arms
3
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