Can a yeast drink boost iron and glow? small study tests it
NCT ID NCT06066151
First seen Jun 26, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This small study tested whether a daily iron-rich yeast drink with SOD can improve anemia and skin condition in women aged 18-35. Eleven women with mild anemia drank the supplement for four weeks. Researchers measured blood iron levels and skin-related markers before and after to see if there was any improvement.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Minayo iron-rich yeast drink with SOD (dietary supplement)
- What this could lead to
- If it works, this could point toward a dietary supplement that helps improve iron levels and skin condition in young women with mild anemia.
- What could go wrong
- This is a very small, early study with only 11 participants and no comparison group, so results may not be reliable or apply to others. It's a supplement, not a drug, and any benefits are likely modest.
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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
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11 people
The number who actually took part.
- Started
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Sep 2023
- Finished
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Dec 2023
- Lead sponsor
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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
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18 to 35 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * Female, aged 18 to 35; * Hemoglobin concentration level below 110g/L based on WHO diagnostic criteria for anemia; * Agree not to take any drugs, supplements, or other dairy products during the trial; * Agree not to take any other medications or supplements containing iron during the trial; * Willing to refrain from participating in other interventional clinical studies during the trial period; * Be able to fully understand the purpose, benefits and potential risks including side effects of the research; * Willing to obey all test requirements and procedures; * Informed consent signed. Exclusion Criteria: * Anemia caused by organic diseases; * Subject who is in the treatment of gastrointestinal symptoms; * Lactose intolerance; * Subject who is currently presence of other organic diseases affecting intestinal function, such as history of gastrointestinal resection, colon or rectal cancer, inflammatory bowel disease, diabetes, hyperthyroidism or hypothyroidism, congenital megacolon, scleroderma, anorexia nervosa, etc.; * Controlling diet, exercising, or taking medications to control weight or affect appetite in the last 3 months; * Subject who has any of the following medical history or clinical findings that may affect the evaluation of the trial effect: significant gastrointestinal disorders, liver, kidney, endocrine, hematological, respiratory and cardiovascular diseases; * Abuse alcohol or other drugs, supplement or OTC drugs currently or n the past may cause bowel dysfunction or can affect test result evaluation; * Frequently use of medications that may affect gastrointestinal function or the immune system according to investigator's judgment; * Take laxatives or other substances that promote digestion 2 weeks before the trail start; * Subject who used drugs or supplements of iron agent 10 days before the beginning of the trial; * Pregnant or lactating women or those planning to become pregnant during the trial; * PI deems that subjects could not fully cooperate with trial arrangements.
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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
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Shanghai Raison CMA Lab
Shanghai, Shanghai Municipality, China
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Other studies related to the condition(s) this trial covers.
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