Could probiotics be the next blood pressure remedy?
NCT ID NCT07206303
First seen Jun 25, 2026 · Last updated Sep 01, 2026 · Updated 3 times
Summary
This pilot study is testing whether a Bifidobacterium probiotic supplement can help lower blood pressure in 30 middle-aged Chinese adults with untreated hypertension. Participants will take the probiotic for 12 weeks, and researchers will monitor their blood pressure and other health markers. The goal is to see if this approach is promising enough for a larger trial.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Bifidobacterium-based probiotics
- What this could lead to
- If it works, this could point toward a simple, natural way to help manage blood pressure without medication.
- What could go wrong
- This is a very small, early pilot study with only 30 people. It may not show a clear effect, and results may not apply to other groups.
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
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Nov 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2027
An estimate. End dates often move.
- Lead sponsor
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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
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40 to 65 years
- Sex
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Anyone
- Healthy volunteers
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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 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: * Men or women, aged 40-65 years old. * Chinese residing in Hong Kong. * Clinic SBP ≥130mmHg according to screening measurement at baseline. * Untreated or not on antihypertensive medications within 4 weeks. * Able to provide informed consent. Exclusion Criteria: * Clinic SBP \>165mmHg according to screening measurement at baseline * Known history of diabetes, coronary artery disease, stroke, peripheral artery disease, malignancy or chronic kidney disease * Known history of gastrointestinal disorders including inflammatory bowel disease, irritable bowel syndrome, Helicobacter pylori infection, liver cirrhosis or long-term use of proton pump inhibitors. * Known increased risk of infection due to endovascular or rheumatic heart disease, endovascular grafts, congenital heart defects, endocarditis, mechanical heart valves, and permanent endovascular devices including permanent (not temporary) hemodialysis catheters, pacemakers, or defibrillators. * Known secondary causes of hypertension. * Currently taking omega-3 fatty acid supplements, probiotics, rifaximin, steroids, and antihypertensive agents within 4 weeks. * Currently taking antibiotics within 6 months. * Currently taking anti-oxidant vitamins within 6 months. * Recent travel to tropical areas within 6 months. * Recent bariatric surgery, hepatic resection, intestinal resection/colectomy, or any surgery within 3 months before the study. * Identified higher susceptibility to infections caused by immunosuppression, such as a history of organ or hematopoietic stem cell (HSCs) transplant, neutropenia (ANC \<500 cells/µl), HIV, and CD4 \<200 cells/µl. * Known allergies to any of the components of Bifidobacterium-based probiotics supplement. * Women who are pregnant, or intending to become pregnant, or lactation. * Intending to participate or have participated in a clinical or nutritional intervention study in the last 30 days before study enrolment.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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The University of Hong Kong
Hong Kong, Hong Kong
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