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RecruitingNCT07226414

Prenatal Study in Healthy Pregnant Women

Evaluating the Impact of Perelel Prenatal on Biomarkers in Healthy Pregnant Women.

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Perelel Inc. · Industry
Sex
Female
Age
21 Years – 40 Years
Healthy volunteers
Not accepted

Summary

Clinical Trial Summary The goal of this clinical trial is to address the impact of a gummy prenatal vs a capsule based prenatal in pregnant women. The main question it aims to answer is: Does 12-week daily administration of Prenatal Capsule affect serum iron levels in pregnant women in their second trimester compared to a comparator gummy prenatal? Researchers will compare Prenatal Capsule to a comparator Prenatal Gummy to see if there are differences in serum iron levels after 12 weeks of daily use. Participants will: Take their assigned prenatal supplement (either Prenatal Capsule or the comparator Prenatal Gummy) daily for 12 weeks Be in their second trimester of pregnancy during the study period Have their serum iron levels measured at baseline and after the 12-week intervention period

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTPrenatal CapsuleThis study will look at the impacts of a prenatal capsule vs a gummy comparator prenatal. The prenatal consists of 2 multivitamin + micronutrient blend with one omega softgel.
DIETARY_SUPPLEMENTPrenatal GummyThis prenatal gummy is a commercially available multivitamin that also contains omega-3 DHA and EPA

Timeline

Start date
2025-12-01
Primary completion
2026-09-01
Completion
2026-11-01
First posted
2025-11-10
Last updated
2025-12-18

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07226414. Inclusion in this directory is not an endorsement.