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Which iron pill works best? small study tests natural vs. standard supplements

NCT ID NCT07563686

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
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This completed study looked at how well healthy pre-menopausal women with low iron stores absorb iron from two different supplements: Spatone (a natural iron-rich water) and ferrous sulphate (a standard iron pill). Fourteen women took three different doses (5, 10, and 15 mg) of each supplement in a random order. Researchers measured iron absorption by tracking a special stable isotope in the blood. The goal was to see which supplement and dose provides the best iron uptake, which could help guide dietary recommendations for iron deficiency.

What this could mean

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

Active substance
Spatone (natural iron-rich water) and ferrous sulphate (standard iron supplement)
What this could lead to
If it works, this could help identify which iron supplement is better absorbed, potentially improving dietary advice for women with low iron.
What could go wrong
This is a small, early-stage study with only 14 participants, so results may not apply to everyone. It measures absorption in a lab setting, not real-world effectiveness.

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

14 people

The number who actually took part.

Started

Jan 2024

Finished

Jan 2026

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

19 to 49 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 pre-menopausal women * Aged 19-49 years * With low iron stores (below 30 μg/L serum ferritin; normal range 30-100 μg/L). Exclusion Criteria: * Allergy to iron supplements * BMI above 25 * Pregnant * Post-menopausal women * History of alcohol or substance abuse * Reported history of CVD, diabetes, cancer, kidney, liver or intestinal disease, gastrointestinal disorder * Use of drugs likely to alter gastrointestinal function * Donated blood recently (within the last 3 months prior to screening visit)

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • King's College London

    London, Greater London, SE1 9NH, United Kingdom

More trials for these conditions

Other studies related to the condition(s) this trial covers.