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Eggs vs. dairy: new study tests which boosts choline best for women over 50

NCT ID NCT06902480

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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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 Results may not be published yet.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)

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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

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Status unknown
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First seen Jun 27, 2026 · Last updated Aug 28, 2026 · Updated 4 times

Summary

This study looks at how well the body uses choline from a new dairy ingredient compared to eggs in women aged 51-70 who have gone through menopause. Participants will drink a chocolate-flavored drink with either the dairy ingredient or whole egg powder. The goal is to see if dairy can be a good source of choline, an important nutrient.

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 24 people

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

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Dec 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.

Ages

51 to 70 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: * Ages between 51 and 70 * Is currently post-menopausal (Post-menopausal is a term used to describe the time in a woman's life after she has gone through menopause. This usually happens between the ages of 45 and 55. Menopause is when a woman's menstrual periods stop permanently (at least 12 months)) * Not allergic to the intervention foods and allergens that are related to the production of intervention foods (e.g. dairy products, egg, fish, peanut, shellfish, soy, tree nuts, wheat, crustaceans, gluten, mollusks, mustard, sesame seeds.) * Had stable body weight (± 5%) for the past 6 months * Free from cancer * Did not have weight loss surgery, colon surgery * Do not have chronic kidney diseases * Do not have malabsorption towards fat and dairy products * Willing to complete health surveys * Willing to complete two 4-day food diaries * Willing to consume the intervention smoothies * Willing to provide blood, urine, fecal samples at baseline and after 10 days of intervention Exclusion Criteria: * On weight loss/weight gain diets * Diagnosed with fat malabsorption * Undergoing weight loss surgery * Diagnosed with chronic kidney diseases * Allergic to the intervention foods and allergens that are related to the production of intervention foods (e.g. dairy products, egg, chocolate, fish, peanut, shellfish, soy, tree nuts, wheat, crustaceans, gluten, mollusks, mustard, sesame seeds, banana, strawberry, raspberry, blackberry, blueberry.) * Regularly using antibiotics or probiotics or prebiotics * Regularly using weight-loss drugs (GLP-1, Orlistat, Cetilistat, etc.) * Regularly using laxatives * Unable to avoid strenuous exercise during the study (\>4 h vigorous exercise per day)

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As listed by the trial registrant

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How to take part

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  2. The official record

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Contacts and locations

Locations

  • University of Wisconsin - Madison

    Madison, Wisconsin, 53705, United States

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