Can a daily capsule keep knees happy? a supplement blend puts joint health to the test
NCT ID NCT07729657
First seen Jul 27, 2026 · Last updated Jul 28, 2026 · Updated 1 time
Summary
This trial is testing whether a dietary supplement containing N-acetylglucosamine (NAG), hyaluronic acid (HA), and pyrroloquinoline quinone (PQQ) can reduce knee pain and improve physical function in healthy Japanese adults with low muscle mass and mild knee discomfort. Participants take three capsules daily for 12 weeks and complete questionnaires, strength tests, and walking assessments. Researchers compare the supplement blend against a placebo to see if it truly helps.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a dietary supplement containing N-acetylglucosamine (NAG), hyaluronic acid (HA), and pyrroloquinoline quinone (PQQ)
- What this could lead to
- If the supplements prove effective, they could offer a simple, non-drug option for supporting joint health and mobility in people with early knee discomfort.
- What could go wrong
- This is an early-stage trial with a small number of participants. The supplements may show no meaningful benefit over placebo, and individual results may vary.
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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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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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jul 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2026
An estimate. End dates often move.
- 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 years and older
- Sex
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Anyone
- 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: 1. Japanese 2. Men or women 3. Adults 4. Healthy individuals 5. Individuals whose body mass index is ≥18.5 and \<30 kg/m2 6. Individuals who have low whole-body muscle mass 7. Individuals with KL grades of 0 or I on radiographic examination 8. Individuals with high knee pain intensity using the JKOM, as measured by VAS Exclusion Criteria: 1. Individuals receiving treatment for or have a history of malignant tumors, heart failure, or myocardial infarction 2. Individuals with an implanted pacemaker or implantable cardioverter-defibrillator 3. Individuals undergoing treatment for any of the following chronic diseases: cardiac arrhythmia, liver disorder, chronic kidney disease, cerebrovascular disorder, rheumatic disease, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases 4. Individuals consuming Foods for Specified Health Uses (FOSHU) or FFC 5. Individuals taking or using medications (including herbal medicines) or supplements 6. Individuals who are allergic to medications or foods related to the test product 7. Individuals engaging at least 60 minutes per week in physical activity that induces heavy breathing and sweating 8. Individuals engaging in strength training (including bodyweight exercises such as push-ups), running, walking, cycling, or swimming at least twice a week 9. Individuals who are pregnant, lactating, or planning to become pregnant during the study period 10. Individuals usually taking FOSHU or FFC, e.g., NAG, proteoglycan from salmon nasal cartilage (SNC), undenatured type II collagen from SNC, glucosamine hydrochloride, curcumin, elastin peptide from skipjack, or collagen peptide 11. Individuals engaging in intense knee joint-loading exercise (e.g., ball sports, such as soccer, baseball, and basketball, jogging, running, skiing, or snowboarding) 12. Individuals who use a cane or joint support, or may use them during this study 13. Individuals deemed unsuitable to participate in this study by the principal investigator
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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
2 sites. 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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Medical Corporation Seishinkai, Takara Clinic
Shinagawa-ku, Tokyo, 141-0022, Japan
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Nerima Medical Association Minami-machi Clinic
Nerima-ku, Tokyo, 176-0002, Japan