Prenatal Nutrient Status Study

NCT ID: NCT06156826

Last Updated: 2024-10-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

502 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-11-07

Study Completion Date

2024-09-04

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this research is to gather data on nutritional status from approximately 250 pregnant women who are currently taking a prenatal vitamin in order to better understand if the prenatal vitamins that most people use are providing enough nourishment during pregnancy.

Participants will be asked to:

* complete an online survey
* schedule a blood draw for the Study Multivitamin Blood Test
* complete the blood draw visit
* complete a final survey at study end

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Pregnancy Related Nutrient Deficiency

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* 18 years of age or older
* Speaks, reads, and understands English
* Lives in the United States
* Lives within a ZIP code from the metropolitan areas where mobile phlebotomists will be available for blood draws
* Assigned female sex at birth
* Currently within weeks 24-34 of pregnancy
* Currently taking a daily prenatal vitamin

Exclusion Criteria

* Birth sex other than female
* Currently taking a prenatal vitamin without Folic Acid other than Needed Prenatal Multivitamin
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Needed PBC

INDUSTRY

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Ari Calhoun, ND

Role: PRINCIPAL_INVESTIGATOR

Wholesome Brain Medicine

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Needed PBC

Los Angeles, California, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

ND.001

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Vitamin D and Preeclampsia
NCT01648842 COMPLETED
Mother Infant Nutrition Study
NCT04132310 ENROLLING_BY_INVITATION
Low Dose Calcium to Prevent Preeclampsia
NCT02338687 COMPLETED PHASE4
Family Study on Preeclampsia
NCT00344162 COMPLETED