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Clinical Effectiveness Study Project of Glucosamine Chondroitin Tablets

Clinical Effectiveness Study Project of Glucosamine Chondroitin Tablets

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000320
Enrollment
Unknown
Registered
2026-02-09
Start date
2025-08-01
Completion date
Unknown
Last updated
2026-03-02

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

Conditions

knee osteoarthritis

Interventions

control group:The subjects took the placebo for 90 days.
Experimental group:The subjects took the glucosamine chondroitin tablets for 90 days.

Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1: 40 - 70 years old, gender not restricted. 2: Diagnosed with knee osteoarthritis: 1) Repeated knee pain within the past month, accompanied by the following two conditions, 2) Age = 50 years old, 3) Presence of bone friction sounds (feeling) during activity, 4) Morning stiffness duration = 30 minutes, 5) Kellgren & Lawrence classification: Grade 0 - III, meeting any two of the above conditions (1), 2), 3), 4), 5)). 3: Those with normal liver and kidney functions. 4: Voluntary signing of the informed consent form.

Exclusion criteria

Exclusion criteria: 1: Symptoms have worsened. Those who have taken or need to take non-steroidal anti-inflammatory drugs. 2: Individuals who are allergic to multiple medications or to the known components of the product under study. 3: Women who are pregnant or planning to get pregnant, are currently pregnant, or are in the lactation period within the past six months. 4: Diseases that affect the joints include conditions such as psoriasis, syphilitic neuropathy, xanthelasma, metabolic bone diseases, and acute trauma. 5: Patients with severe heart, brain, liver, kidney and hematopoietic system diseases, as well as those with serious occupational diseases and mental disorders. 6: Individuals who take items related to the tested function within a short period of time and whose judgment is thereby affected. 7: Those whose complaints are unclear, those with weak constitutions unable to undergo the test, and those who fail to use the test samples as per the regulations

Design outcomes

Primary

MeasureTime frame
WOMAC Score;Clinical symptom score in traditional Chinese medicine;Kellgren & Lawrence classification;

Secondary

MeasureTime frame
VAS pain score;Inflammatory indicators (interleukin-1ß, interleukin-6, tumor necrosis factor-a);

Countries

China

Contacts

Public ContactYao Jjiamei

Xiangya Hospital, Central South University

yjmmjy@126.com13787105601

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Mar 14, 2026