Skip to content

A randomized controlled trial for improving knee joint pain in human

A randomized controlled trial for improving knee joint pain in human - A randomized controlled trial for improving knee joint pain in human

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000014324
Enrollment
96
Registered
2014-06-20
Start date
2014-06-20
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 adults

Interventions

Duration: 8 weeks Test material: Boswellin Super 300 mg One tablet per day (300 mg/day) Duration: 8 weeks Test material: 449 mg One tablet per day (449 mg/day) Duration: 8 weeks Test material: 44

Sponsors

ORTHOMEDICO Inc.
Lead Sponsor
Seishin-kai Medical Association Inc, Takara Medical Clinic.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: a) Healthy adults, who have knee joint pain b) Persons who are 60s, 50s, 40s, 30s and 20s

Exclusion criteria

Exclusion criteria: a) Persons who have previous medical history of malignant tumor, or heart failure and/or myocardial infarction b) Patients being treated for at least one of following diseases atrial fibrillation, cardiac arrhythmia, hepatic disorder, renal disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, and/or other chronic disease c) Persons who take medicines, herbal medicines, or dietary supplements d) Persons who are allergic to medicines, or foods related to the test material of this trial e) Pregnant women, lactating women, or women who want to get pregnant during the trial period f) Persons who have been enrolled in the other clinical trials within last 3 months before the agreement for the participation to this trial g) Persons who are judged not suitable to participate in this trial by physician.

Design outcomes

Primary

MeasureTime frame
Questionnaires (JKOM)

Secondary

MeasureTime frame
Serum Hyarulonic acid Serum hs-CRP Questionnaires (Likert scale) Questionnaires (WOMAC) Blood test Urianalysis Physical examinations

Countries

Japan

Contacts

Public ContactNaoko SUZUKI

ORTHOMEDICO, Inc. R&D Department

nao@orthomedico.jp03-3818-0610

Outcome results

None listed

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