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Pregnancy supplement may shape Child's attention and social skills

NCT ID NCT03028857

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested whether giving pregnant women a nutritional supplement called phosphatidylcholine could improve their child's brain development. About 216 healthy pregnant women took either the supplement or a placebo from around 16 weeks of pregnancy until birth. Researchers then checked the children's behavior, attention, and social skills at age 4, along with other developmental areas like motor and language skills.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Phase 1

The first testing in people. Mainly checks safety and dose, usually in a small group.

Participants

216 people

The number who actually took part.

Started

Jun 2017

Finished

Dec 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 45 years

Sex

Female participants only

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * General Health: Other than pregnancy related illnesses, physically healthy expectant mothers * ages 18-45 years * prepregnancy BMI\>18 and \<45 Exclusion Criteria: * Prior history of fetal death * Current personal history of chronic infections, including HIV * Current personal or family history out to first degree relatives of 1. Trimethylaminuria 2. Homocystinuria * Primary language other than English or Spanish * Evidence of noncompliance

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • Saint Joseph Hospital

    Denver, Colorado, 80218, United States

  • UCHealth

    Aurora, Colorado, 80045, United States

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