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Experts unite to create safer supplement rules for pregnant women

NCT ID NCT07296562

Knowledge-focused Sponsor: Venus Research Center Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

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 This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 aims to create clear, expert-backed recommendations for using vitamins, minerals, and other supplements during pregnancy. Currently, there is a lot of variation in how doctors prescribe these products. The study will involve 15 specialists who will answer questions in multiple rounds to reach agreement on safe and effective use.

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.

Participants

About 15 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Sep 2027

An estimate. End dates often move.

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.

Who is studied

he study population will consist of a purposive sample of experts in obstetrics, maternal-fetal medicine, and clinical nutrition who are actively involved in prenatal care and have experience or knowledge regarding the use of nutriceuticals in pregnancy. Panel Size and Rationale: Target enrollment: 20-35 experts. Sufficient to capture diverse perspectives while remaining feasible for multiple Delphi rounds. Minimum for analysis: 15 panelists, ensuring representativeness in case of attrition.

Ages

25 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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: * Board-certified obstetricians, maternal-fetal medicine specialists, or clinical nutritionists with ≥5 years of relevant clinical experience. Active involvement in prenatal care and experience or knowledge in nutriceutical use during pregnancy. Engagement in clinical teaching, research, guideline development, or professional society activities related to maternal health or nutrition. Willingness and availability to participate in all Delphi rounds. Provision of informed consent to participate. Exclusion Criteria: * Non-obstetric or non-nutrition specialty. Less than 5 years of relevant clinical experience. Limited or no experience with nutriceutical counseling/prescribing in pregnancy. Significant undisclosed conflict of interest related to nutriceutical products. Inability or unwillingness to participate in all Delphi rounds.

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As listed by the trial registrant

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

Nutraceuticals Pregnancy

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    The full official record for this study. This one lists no contact details, but it is the first place any would appear.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Venus Research Center

    Cairo, Egypt

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