🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in the USA / NCT07226414
Recruiting Not applicable

Prenatal Study in Healthy Pregnant Women

NCT07226414 · tracked via the Priya Life Science USA tracker
Sponsor
Perelel Inc.
Phase
Not applicable
Started
2025-12-01
Last updated
2025-12-18

Condition(s) studied

Pregnancy

Investigational drug(s) / intervention(s)

Prenatal CapsulePrenatal Gummy

Prenatal Capsule: This 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.

Prenatal Gummy: This prenatal gummy is a commercially available multivitamin that also contains omega-3 DHA and EPA

Study 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

Eligibility

Sex
FEMALE
Min age
21 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: * Be able to give written informed consent. * Healthy pregnant women between 21- 40 years of age (inclusive). * Pregnant women in the second trimester of pregnancy (gestational age of 14-19 weeks). * Willing to consume the Study Product daily for the duration of the study. Exclusion Criteria: * History of drug or alcohol abuse * Is hypersensitive to any of the contents of the study product, that would preclude intake of the study products. * Has any significant acute or chronic coexisting health conditions that would prevent them from fulfilling the study requirements, put the Participant at risk, or would confound the interpretation of the study results as judged by the investigator on the basis of medical history. * Severe nausea and vomiting in the first trimester, including hyperemesis gravidarum (HG) * Inability to tolerate oral supplement intake due to gastrointestinal symptoms during the first trimester of pregnancy * Prior Pregnancy Complications (gestational diabetes (GD), HG, or pre-eclampsia, NTDs (Neural Tube Defects)) * Current pregnancy complications (GD, Iron Deficiency Anemia) * Hypertension * Diabetes mellitus * Cardiovascular disease * Class II/III obesity (defined as BMI ≥35.0 Kg/m2) * Malabsorption syndromes (e.g., celiac disease, inflammatory bowel disease) * Severe anemia or iron overload disorders * Thyroid disorders * Current or recent (in the past 12 weeks prior to Visit 1) use of a medication that the investigator believes would interfere with the objectives of the study or pose a safety risk or confound the interpretation of the study results, as judged by the investigator. Prohibited medications include: Medications that contain fat-soluble vitamins A, E, or K in high doses \- Current or recent (in the past 12 weeks prior to Visit 1) use of prohibited nutritional or non-nutritional supplements that the investigator believes would interfere with the objectives of the study or pose a safety risk or confound the interpretation of the study results as judged by the investigator.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Atlantia Clinical Trials, Chicago Chicago Illinois Recruiting
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 NCT07226414 on ClinicalTrials.gov ↗ ← All trials in the USA