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A Study of Two Approved Drugs in Patients With Osteoarthritis (0966-219)

Phase 3
Completed
Conditions
Osteoarthritis
Registration Number
NCT00092352
Lead Sponsor
Merck Sharp & Dohme LLC
Brief Summary

The purpose of this study is to compare the safety and effectiveness of two approved drugs in the treatment of osteoarthritis of the knee.

Detailed Description

The duration of treatment is 6 weeks.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
395
Inclusion Criteria
  • Osteoarthritis of the knee which requires treatment with medication for pain relief
Exclusion Criteria
  • Any known allergy to the study drug

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Osteoarthritis (OA) of the knee as measured by Patient Global Assessment of Response to Therapy (PGART) and WOMAC VA 3.0 over 6 weeks of treatment.
Secondary Outcome Measures
NameTimeMethod
WOMAC Question #1 over 6 wks of treatment.
OA of the knee as measured by PGART over 6 wks of treatment.
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