Effects of Aquamin F on NSAID Dose Reduction in Osteoarthritis of the Knee

Inclusion criteria

• Subjects aged 35 to 75, male or female
• Subjects diagnosed with symptomatic moderate to severe osteoarthritis of the knee according to the modified criteria of the American College of Rheumatology 17,18
• Subjects who present with osteoarthritis of the knee as judged by symptoms and disabilities detectable through published, validated questionnaires or previous diagnosis by a physician
• subjects who are symptomatic with daily or near daily pain and stiffness from osteoarthritis
• subjects who are taking non-steroidal anti-inflammatory drugs (NSAIDs) prior to study enrollment
• subjects who are willing to stop NSAIDS and use acetaminophen for pain management during the trial
• subjects with screening WOMAC osteoarthritis index total score (transformed score) of not more than 75
• subjects with ability to comprehend and complete the questionnaires and forms
• subjects whose schedules permit clinical evaluations every four weeks
• subjects who are willing to stop taking calcium supplements, if any and to restrict consumption of high calcium food to 600mg (two dairy servings) per day
• subjects with a high probability of compliance with study procedures and test article consumption
• subjects willing and able to follow protocol guidelines and schedules and complete diaries
• subjects who are likely to abstain from taking unathorized supplements or participating in any other clinical trial or experimental treatment during this trial
• subjects with normal gastrointestinal digestion and absorption

Exclusion criteria

• subjects who have a history of inflammatory arthritis, gout, pseudogout, Paget's disease, seizure disorder, insulin dependent diabetes mellitus, uncontrolled hypertension, unstable cardiovascular disease, active hepatic or renal disease, active cancer and/or HIV infection
• subjects who are non-ambulatory or bedridden due to osteoarthritis
• subjects who are dependent on prescription drugs to control pain
• subjects on any other clinical trial or experimental treatment in the past 3 months
• subjects who are pregnant, lactating or at risk of becoming pregnant
• subjects who have received : intramuscular corticosteroid injection or systemic corticosteroid administration within 4 weeks prior to study enrollment, intra-articular corticosteroid injection within 2 months prior to study enrollment or intra-articular hyaluronic acid injection within 4 months prior to study enrollment.