Effects of Aquamin F on Osteoarthritis of the Knee

Method: Subjects were randomized to receive 12 weeks of Glucosamine sulfate vs Aquamin F vs Placebo vs Aquamin F + Glucosamine sulfate while controlling for pain with acetaminophen. Subjects were then followed for blood chemistry measurements only over an additional 12-week period specifically to assess blood calcium levels post treatment. All participants were subjected to the same diet and exercise regimen and measurements included: WOMAC scores (pain, stiffness, mobility, total score), 6 Minute Walking Distances, active and passive range of motion measurements, DXA scans, blood chemistry, hematology, CRP levels and lipid profiles as well as rescue medication diary measurements and adverse event assessments. An independent statistician analyzed the data using independent t-tests and ANCOVA for between-group comparisons and matched-pair t-tests for within-group comparisons of patients included in ITT-LOCF and completer analyses.

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 Rheumatology17, 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 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 clinic evaluations every four weeks.
• Subjects who are willing to stop taking calcium supplements, if any, and to restrict consumption of high calcium foods to 600 mg (two dairy serving) 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 unauthorized supplements or participating in any other clinical trial or experimental treatment during this trial
• Subjects with normal gastrointestinal digestion and absorption.

Exclusion criteria

• Subjects suffering from 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:

• Non-Steroidal Anti-Inflammatory Drugs (NSAIDS) within 48 hours prior to study enrollment.
• Intramuscular or systemic corticosteroid injection within 4 weeks prior to study enrollment.
• Intra-articular corticosteroid injection within 2 months prior to study enrollment.
• Intra-articular hyaluronic acid injection within 4 months prior to study enrollment.