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The observation of knee joint before and after supplement intake

The observation of knee joint before and after supplement intake - The observation of knee joint before and after supplement intake

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000039388
Enrollment
8
Registered
2020-02-04
Start date
2020-02-04
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 adult

Interventions

Intake of the supplement once a day for 48 consecutive weeks

Sponsors

KOBAYASHI Pharmaceutical Co.,Ltd
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: Healthy woman with the knee joint discomfort

Exclusion criteria

Exclusion criteria: 1. Subjects with severe pain in joints other than the knee joint 2. Subjects who have a current or previous history of joint disease or serious disease that affects efficacy evaluation 3. Subjects who regularly use medicines and health foods that affect efficacy evaluation 4. Subjects who are judged inappropriate by the investigator

Design outcomes

Primary

MeasureTime frame
None—

Countries

Japan

Contacts

Public ContactTakuya Makino

KOBAYASHI Pharmaceutical Co.,Ltd Central R&D Laboratory

t.makino@kobayashi.co.jp080-3465-2263

Outcome results

None listed

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