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Could a wheat pill ease menopause dryness? new trial seeks answers

NCT ID NCT07386249

Symptom relief Sponsor: Seppic Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a daily capsule made from wheat polar lipids can reduce vaginal dryness in healthy postmenopausal women. 110 women aged 45-65 will take either the supplement or a placebo for 12 weeks. Researchers will measure changes in dryness, vaginal pH, and other menopause symptoms.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
wheat polar lipid complex (dietary supplement)
What this could lead to
If it works, this could offer a natural, non-hormonal option to ease vaginal dryness in postmenopausal women.
What could go wrong
This is an early exploratory study with a small sample size. The supplement may not work better than placebo, and results may not apply to all women.

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

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 110 people

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

Started

Feb 2026

Expected to finish

Nov 2026

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

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

Ages

45 to 65 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: * Healthy woman, aged of 45 to 65 years (inclusive) * In postmenopause, defined according to the STRAW criteria as the absence of menstrual periods for at least 12 consecutive months * Reporting a vaginal dryness intensity score ≥ 4 on a 0-10 Visual Analogue Scale (VAS), and a score ≥ 16 on the Menopause Rating Scale (MRS) * Provision of signed and dated informed consent form * Stated willingness to comply with all study procedures and availability for the duration of the study * Stated willingness to maintain their usual life habits (diet, physical activity, alcohol consumption…) * Speaking French. Exclusion Criteria: * Use of systemic hormonal therapy within the past 3 months * Use of dietary supplements, herbal products, or over-the-counter remedies intended to alleviate menopausal symptoms within 4 weeks prior to the screening visit (wash-out period ≥ 1 month required) * Use of vaginal hormonal formulations within 4 weeks prior to screening * History of hormone-dependent cancers * History of hysterectomy or bilateral oophorectomy * Current alcohol dependence or excessive alcohol consumption exceeding an average of 14 standard drinks per week * Current use of illicit drugs or recent history of drug dependence * Current or previously diagnosed eating disorders considered likely to impact participant safety or study outcomes * Presence of severe or uncontrolled chronic medical conditions, or any acute medical condition judged by the investigator to potentially interfere with the MRS assessment or participant safety * Subject participating in another intervention trial

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As listed by the trial registrant

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

Menopause symptoms Vaginal dryness

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

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

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Contacts and locations

Locations

  • Center of Investigation in Clinical Nutrition (CICN)

    RECRUITING

    Louvain-la-Neuve, Belgium, 1348, Belgium

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