Table 15Efficacy, glucosamine and chondroitin trials

Author, Year
Quality
Condition Number EnrolledComparison
Duration of Study
Main Results
Glucosamine Trials
Herrero-Beaumont, 2007204
Fair
OA of knee
318
Glucosamine sulfate 1500 mg powder for oral solution qd

Acetaminophen 1 gm po tid

Placebo

6 months
Glucosamine sulfate vs. acetaminophen vs. placebo

Change from baseline:
Lequesne Index (0 to 24): −3.1 vs. −2.7 vs. −1.9; p=0.032 for difference vs. placebo

WOMAC total (0 to 100): −12.9 vs. −12.3 vs. −8.2; p=0.039 for difference vs. placebo

WOMAC pain (0 to 100): −2.7 vs. −2.4 vs. −1.8; NS

WOMAC function (0 to 100): −9.2 vs. −8.7 vs. −5.5; p=0.022 for difference vs. placebo

OARSI-A responders: 40% vs. 21.2% for placebo, p= 0.004
Rozendaal, 2008205
Rozendaal, 2009
Good
OA of hip
222
Glucosamine sulfate 1500 mg po qd or bid

Placebo

24 months
Glucosamine sulfate vs. placebo

Change from baseline:

WOMAC pain (0 to 100): −1.90 ± 1.6 vs. −0.30 ± 1.6, adjusted difference −1.54 (−5.43 to 2.36)
WOMAC function (0 to 100): −1.69 ± 1.3 vs. 0.38 ± 1.3, adjusted difference −2.01 (95% CI −5.38 to 1.36)

JSN, mm adjusted difference:
Minimal: −0.029 (95% CI −0.122 to 0.064)
Lateral: −0.017 (95% CI −0.121 to 0.088)
Superior: 0.016 (95% CI −0.079 to 0.111)
Axial: −0.005 (95% CI −0.118 to 0.108)
Wilkens, 2010206
Good
Degenerative lumbar OA
250
Glucosamine sulfate 1500 mg po qd or tid

Placebo

6 months
Glucosamine sulfate vs. placebo

Treatment Effect at 1 year (negative values favor glucosamine):

RMDQ (0 to 24): −0.8 (95% CI −2.0 to 0.4), p=0.50

NRS LBP (0 to 10): −0.3 (95% CI −0.8 to 0.3). p=.85

Global perceived effect, No. (%):* 34 (30.9%) vs. 32 (29.4%), p=.30
Chondroitin Trials
Kahan, 2009207
Fair
OA of knee
622
Chondroitin sulfates 4 & 6 800 mg every evening

Placebo

2 years
Chondroitin sulfate vs. placebo

At 6 months:
WOMAC pain score decrease ≥40%: 41% vs. 34%, p=0.05
No difference in WOMAC total, stiffness, or function

At 24 months: minimum JSW loss (mean ± SEM): −0.07 ± 0.03 mm vs. −0.31 ± 0.04 mm
Hodges-Lehmann estimator of median effect of treatment: −0.14 (95% CI 0.06 – 0.21 mm, p<0.0001)
Mazieres, 2010208
Fair
OA of knee
307
Chondroitin sulfate 500 mg po bid

Placebo

24 weeks
Chondroitin sulfate vs. placebo

Change from baseline to week 24, M (SD):

Lequesne Index, (0 to 24): −2.4 (3.4) vs. −1.7 (3.3), p=0.109

VAS pain, mm: −26.2 (24.9) mm vs. −19.9 (23.5) mm, p= 0.029

OMERACT-OARSI responders: 68% vs. 56% (p=0.03)
Michel, 2005209
Fair
OA of knee
300
Chondroitin sulfates 4 & 6 800 mg po qd

Placebo

2 years
Chondroitin sulfate vs. placebo

Changes in WOMAC:
Total: −3.9% vs. 2.1%
Pain: −11.0% vs. −6.2%
Stiffness: −7.8% vs. −4.6%
Function: −0.8% vs. 5.9%

JSN Minimum difference: 0.12 (95% CI 0.00 to 0.24), p=0.05

JSM Mean difference: 0.14 (95% CI 0.01 to 0.27), p =0.04
Moller, 2010210
Fair
OA of knee (in patients with psoriasis)
129
Chondroitin sulfate 800 mg po qd

Placebo

3 months
Chondroitin sulfate vs. placebo (mean differences at 3 months)

Pain intensity (0 to 100 mm VAS): −12 (95% CI −20 to −4)
Lequesne Index (0 to 24): −1.7 (95% CI −3.0 to −0.4)
SF-36 physical component (0 to 100): 1.7 (95% CI 1.4 to −1.2)
SF-36 mental component (0 to 100): −0.3 (95% CI −3.3 to 2.6)
Glucosamine/Chondroitin Trials
Messier, 2007211
Fair
OA of knee
89
Glucosamine hydrochloride 1500 mg and Chondroitin sulfate 1200 mg qd or tid

Placebo

1 year; 6 months alone; 6 months treatment plus exercise
Glucosamine hydrochloride + chondroitin sulfate vs. placebo

At 12 months:
WOMAC pain (0 to 20): 6.0 (0.5) vs. 5.18 (0.5)

WOMAC function (0 to 68): 19.4 (1.2) vs. 20.6 (1.2)b
Sawitzke, 2008212
Good
OA of knee
662
Glucosamine sulfate 500 mg tid

Chondroitin sulfate 400 mg tid

Combination of Glucosamine and Chondroitin

Celecoxib 200 mg qd

Placebo

24 months
Glucosamine hydrochloride vs. chondroitin sulfate vs. both vs. placebo

Mean loss in JSW over 2 years: 0.013 vs. 0.107 vs. 0.194 vs. 0.111 vs. 1.166

Difference from placebo (negative value = less JSW loss): −0.153 (−0.379, 0.074) vs. −0.059 (−0.287, 0.169) vs. 0.028 (−0.214,0.271) vs. −0.055 (−0.279, 0.170)

Disease progression over 2 years, % of patients:18.6 vs. 21.4 vs. 24.4 vs. 20.2 vs. 22.4

bid = twice daily; JSM = joint space measurement; JSN = joint space narrowing; JSW = joint space width; NRS LBP = numerical rating scale for low back pain; OA = osteoarthritis; OMERACT-OARSI = Outcomes Measures in Arthritis Clinical Trials-Osteoarthritis Research Society International; po = orally; RMDQ = Roland Morris Disability Questionnaire; qd = once daily; qid = four time daily; tid = three times daily; VAS = visual analogue scale; WOMAC = Western Ontario and McMaster Universities Osteoarthritis Index

*

Proportion of patients who had a global perceived effect to the intervention

From: Results

Cover of Analgesics for Osteoarthritis
Analgesics for Osteoarthritis: An Update of the 2006 Comparative Effectiveness Review [Internet].
Comparative Effectiveness Reviews, No. 38.
Chou R, McDonagh MS, Nakamoto E, et al.

NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.