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Completed

NCT Number: NCT00928837

Study of Flavocoxid (Limbrel) Versus Naproxen in Subjects With Moderate-Severe Osteoarthritis of the Knee

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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Key information

Age range

35 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Alan Kivitz MD

Duncansville, Pennsylvania, 16635, United States

About this study

To compare the efficacy, safety, quality of life and economic impact of flavocoxid vs naproxen.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Major inclusión criteria:

  • Adults of either gender, ages 35-85, in general good health
  • Diagnosed with OA of the knee, K-L Grade 2-3
  • History of positive response to NSAID's or COX-2 inhibitors
  • Able and willing to discontinue other medicinal OA therapies for length of the study (subjects may continue low dose aspirin for cardioprotection)
  • Females of child bearing potential must use acceptable method of birth control

Major exclusion criteria:

  • Unwilling or unable to read and sign informed consent document
  • Pregnant and nursing women
  • History of severe cardiovascular disease including, but not limited to chronic angina, congestive heart failure, uncontrolled hypertension, acute myocardial infarction within past year
  • K-L grade 1 or 4 OA of the target knee
  • chronic bleeding disorder or present use of anticoagulants
  • History of upper G-I bleed in the past 5 years
  • Significant renal disease including nephrotic syndrome, proteinuria >1 gm/24 hrs or serum Creatinine >2.0
  • Any arthritic disease that is or has the potential to affect the knees during the course of the study
  • Any other condition that might confound evaluation of the target joint including, but not limited to, bursitis, tendonitis or internal derangement in or about the knee, gait disturbances (e.g. mechanical, neurological conditions or disorders of the back), fibromyalgia, polyneuropathies, etc.

Treatment and study plan

flavocoxid 500 mg

Dietary Supplement

flavonoid mixture

Other names: Limbrel 500 mg

Naproxen

Drug

non-steroidal anti-inflammatory drug

Other names: naprosyn

Placebo

Other

Placebo

flavocoxid 250 mg

Other

Medical food product

Other names: Limbrel 250 mg

Primary outcomes

  1. to compare the efficacy of 2 doses of flavocoxid with that of naproxen and placebo at 12 weeks

    Time frame: 3 months

    comparison of short WOMAC and timed walk

  2. to compare the safety of 2 doses of flavocoxid with that of naproxen and placebo at 12 weeks

    Time frame: 3 months

    Comparison of FS-36, subject tolerability VAS

Secondary outcomes

  1. to compare the efficacy of 2 doses of flavocoxid with that of naproxen and placebo at 12 weeks

    Time frame: 6 months

    comparison of short WOMAC and timed walk

  2. to compare the safety of 2 doses of flavocoxid with that of naproxen and placebo at 12 weeks

    Time frame: 6 months

    Comparison of FS-36, subject tolerability VAS

Sponsors and collaborators

Lead sponsor

Primus Pharmaceuticals

Industry

Registry information

Official study title

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

Important dates

Study start
2006
Primary completion
2007
Study completion
2007
First posted
Jun 26, 2009
Registry last updated
Dec 13, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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