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The long-term evaluation of glucosamine sulphate (LEGS) study

Among people with symptomatic osteoarthritis of the knee, does glucosamine sulphate, with or without chondroitin, result in reduced knee pain and slowing the rate of joint space narrowing

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12607000433404
Enrollment
600
Registered
2007-08-24
Start date
2007-08-28
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

There is no known cure for OA and no intervention demonstrated to slow disease progression or delay time to joint replacement surgery. Currently patients are managed symptomatically with all clinical guidelines recommending paracetamol as 'the preferred long term oral analgesic'. This recommendation is based on the increased risk of serious gastrointestinal, cardiovascular and renal diseases with long-term NSAIDs use in older people. However, NSAIDs appear to provide better pain relief for patients with more than mild joint pain. Amongst patients with OA, there is much demand for the dietary supplement glucosamine and chondroitin. Marketing has led to the belief these products are able to slow the rate of joint destruction and cartilage loss and help ease joint pain with little risk of side effects. However, the few trials conducted to date have been inconclusive. A total of 600 patients with knee OA will be randomly allocated to glucosamine sulphate and chondroitin sulphate or matching placebo capsules for two years. Participants will be required to take four capsules, once daily for two years. Clinic visits for assessment, including knee radiographs, will be required at the start of the study as well as 1 year and 2 years later. The main outcomes will be the rate of joint space narrowing, knee pain and physical disability. If glucosamine results in slowing disease progression or in reducing pain, the widespread use of this product would effectively decrease pain, disability and possibly NSAIDs-related illnesses amongst the increasing number of people with OA.

Interventions

1. Glucosamine sulphate (1500mg) and chondroitin (800mg): two 750mg glucosamine sulphate capsules and two 400mg chondroitin capsules daily for two years 2. Glucosamine sulphate (1500mg): two 750mg glucosamine capsules and two placebo chondroitin capsules daily for two years 3. Chondroitin (800mg): two 400mg chondroitin capsules and two placebo glucosamine capsules daily for two years

Sponsors

Clinical and Rehabilitation Sciences Research Group, Faculty of Health Sciences
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Factorial
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

Chronic knee pain Loss of medial tibio-femoral joint space

Exclusion criteria

Unstable diabetes

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026