Clinical Trials Directory

Trials / Completed

CompletedNCT00435292

Study of Flavocoxid (Limbrel) vs Naproxen in Subjects With Mod-Severe Osteoarthritis of the Knee

A Double-Blind, Randomized, Placebo Controlled, Parallel Group, Multi Center Study of Flavocoxid ( Limbrel) vs Naproxen in Subjects With Moderate-Severe Osteoarthritis of the Knee

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
350 (actual)
Sponsor
Primus Pharmaceuticals · Industry
Sex
All
Age
35 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Randomized, double-blind, placebo controlled parallel group, multi center study in subjects with moderate-severe osteoarthritis.

Detailed description

This will be a randomized, double blind, placebo controlled, parallel group, multi-center study in subjects with moderate-severe OA. Subjects will be randomized to receive flavocoxid 250 mg bid, flavocoxid 500 mg bid, naproxen 500 mg bid or placebo in a 2:2:2:1 ratio. Subjects will take study materials twice daily for twelve (12) weeks. After the 12 week visit subjects in the placebo arm will be re-randomized to the two flavocoxid arms. All subjects will then continue on the study for an additional 12 weeks. Subjects will keep a diary noting date of onset of symptom change (better or worse), adverse events and cost of all aspects of medical care related directly or indirectly to osteoarthritis. Laboratory studies for inflammatory markers will be drawn and archived at baseline and at the 12 week visit. In addition, a subgroup of subjects will have arthrocenteses performed at baseline and the 12 week visit and the synovial fluid archived for study of intra-articular inflammatory markers.

Conditions

Interventions

TypeNameDescription
DRUGNaproxennonsteroidal anti-inflammatory drug
DIETARY_SUPPLEMENTflavocoxid 250 mgflavonoid mixture
DIETARY_SUPPLEMENTflavocoxid 500 mgflavonoid mixture

Timeline

Start date
2006-04-01
Primary completion
2007-12-01
Completion
2007-12-01
First posted
2007-02-14
Last updated
2015-10-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00435292. Inclusion in this directory is not an endorsement.