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Clinical Study to Evaluate the Efficacy and Safety of Meriva® on Joint and Cartilage health.

A 12 Weeks, Randomized, Double-blind, Placebo-controlled Clinical Study to Evaluate the Efficacy and Safety of Meriva® on Joint and Cartilage health.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0011542
Enrollment
100
Registered
2026-01-27
Start date
2025-03-17
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

None listed

Interventions

Dietary Supplement : Participants in the test group will be assigned to receive the test product containing Meriva® (curcumin extract), while participants in the control group will be assigned to rece

Sponsors

Ildong Bioscience
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Adult men and women aged 45 to 79 years 2. Radiographic evidence of Kellgren–Lawrence Grade I or II in one or both knee joints 3. Knee pain score = 30 mm on a 100-mm Visual Analog Scale (VAS) 4. Provided written informed consent after receiving sufficient explanation of the study

Exclusion criteria

Exclusion criteria: 1. Suspected rheumatoid arthritis or positive rheumatoid factor 2. Participation in another clinical trial within the past 12 weeks 3. History of knee surgery or musculoskeletal disorders affecting the knee, spine, or lower limbs 4. Autoimmune, inflammatory, infectious joint diseases, or gout 5. Recent use of joint-related functional foods or medications that may affect study outcomes 6. Habitual use of central nervous system drugs or narcotic analgesics 7. History of hypersensitivity to the test product or its ingredients 8. Clinically significant hepatic, renal, cardiovascular disease, or malignancy 9. Pregnant or breastfeeding women, or women of childbearing potential not using appropriate contraception 10. Abnormal laboratory findings or uncontrolled hypertension 11. Any condition deemed unsuitable for participation by the investigator

Design outcomes

Primary

MeasureTime frame
WOMAC questionnaire total score

Secondary

MeasureTime frame
VAS(Visual Analogue Scale, 100 mm) pain score;WOMAC subscale score (pain, stiffness, physical function);Inflammatory and joint-related biomarkers (CRP, COX-2, COMP, CTX-II);Walking time (20-m walk test);WOMAC total score and subscale score

Countries

Korea, Republic of

Contacts

Public ContactJunyoung Park

Yonsei University Yongin Severance Hospital

jjunyon@naver.com+82-31-5189-8451

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 7, 2026