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The test of the improvement effect for knee joint of the S-adenosylmethionine-containing food

The test of the improvement effect for knee joint of the S-adenosylmethionine-containing food - The test of the improvement effect for knee joint of the S-adenosylmethionine-containing food

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000015911
Enrollment
30
Registered
2014-12-10
Start date
2014-12-11
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy volunteer

Interventions

SAMe yeast(4weeks) Placebo (4weeks)

Sponsors

Universal Clinical Systems Co., Ltd.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)Healthy males and females aged 35 to 59 years old (2)Subjects who feel discomfort on knee joint since over 3 months ago, and the discomfort are still continuing

Exclusion criteria

Exclusion criteria: (1)Patients under medical treatment (2)Subjects who have previous medical history of drug and/or food allergy (3)Subjects who have hypertension (not less than level 3) (4)Subjects who have previous medical history of the serious diseases (heart, liver, kidney, blood, digestive system,metabolism system) (5)Patients being treated for rheumatoid arthritis (6)Subjects who have disturbance of motility (7)Subjects who use SAMe-containing-foods and/or functional foods that have mitigation or treatment effect for joint pain (e.g., amino acid, protein, vitamin D, chondroitin, collagen, and/or glucosamine), and can't stop using during this trial (8)Subjects who take medicines and plan to take new health foods (9)Subjects who hope for pregnancy in the test duration, pregnant woman, lactating woman (10)Subjects who have been enrolled in the other clinical trials within about last 1 month (11)Subjects whose declaration of application is incorrect clearly (12)Subjects who are judged as unsuitable for the trial by the investigator or subinvestigator for other reasons

Design outcomes

Primary

MeasureTime frame
Questionnaires(VAS, bodily sensation)

Countries

Japan

Contacts

Public ContactNoriko YAMANAKA

Omnica Co.,Ltd Research team

yamanaka@omnica.co.jp03-5840-9811

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026