Alan Kivitz MD
Duncansville, Pennsylvania, 16635, United States
NCT Number: NCT00928837
The purpose of the study is to compare the efficacy and safety of flavocoxid (Limbrel) with Naproxen and placebo in OA of the knee.
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Notify Me35 year–85 year
All sexes
Interventional
Not applicable
Duncansville, Pennsylvania, 16635, United States
To compare the efficacy, safety, quality of life and economic impact of flavocoxid vs naproxen.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Major inclusión criteria:
Major exclusion criteria:
flavonoid mixture
Other names: Limbrel 500 mg
non-steroidal anti-inflammatory drug
Other names: naprosyn
Placebo
Medical food product
Other names: Limbrel 250 mg
Time frame: 3 months
comparison of short WOMAC and timed walk
Time frame: 3 months
Comparison of FS-36, subject tolerability VAS
Time frame: 6 months
comparison of short WOMAC and timed walk
Time frame: 6 months
Comparison of FS-36, subject tolerability VAS
Primus Pharmaceuticals
Industry
A Double-Blind,Randomized, Placebo Controlled, Parallel Group, Multi-Center Study of Flavocoxid (Limbrel) Versuss Naproxen in Subjects With Moderate-Severe Osteoarthritis of the Knee
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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