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NCT01188213 Clinical Trial

Efficacy of Methylsulfonylmethane Supplementation on Osteoarthritis of The Knee: A Randomized Controlled Study

Knee Osteoarthritis Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01188213
Other study ID # 13/05
Secondary ID
Status Completed
Phase N/A
First received August 21, 2010
Last updated August 24, 2010

Study information
Verified date May 2005
Source Assaf-Harofeh Medical Center
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

The aim of this study was to determine the efficacy of methylsulfonylmethane (MSM) in treating patients with knee OA.

Recruitment information / eligibility
Status Completed
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers
Gender Both
Age group 40 Years to 70 Years
Eligibility Inclusion Criteria:

- symptomatic knee OA for at least 6 months according to the clinical criteria of the American College of Rheumatology (ACR)

- radiographic confirmed knee OA according to the Kellgren & Lawrence scale

Exclusion Criteria:

- acute septic arthritis

- inflammatory arthritis

- any other type of arthritis

- history of knee buckling or recent knee injury

- lack of physical or mental bility to perform or comply with the treatment procedure

- diabetes mellitus

- fibromyalgia or other chronic pain syndromes

- concurrent anti-coagulant/anti-platelet drugs

- arthroscopy or intra-articular injections in the previous 3 months

Study Design

N/A

Related Conditions & MeSH terms

Intervention

Dietary Supplement:
• Methylsulfonylmethane (MSM)

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Assaf-Harofeh Medical Center

Outcome
Type Measure Description Time frame Safety issue
Primary WOMAC questionnaire
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