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Clinical Trial Summary

The primary purpose of this study is to determine if duloxetine 60 mg once daily (QD) reduces pain severity in patients with osteoarthritis (OA) knee pain compared with placebo.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00945945
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 3
Start date July 2009
Completion date May 2010

See also
  Status Clinical Trial Phase
Completed NCT01018680 - A Study Comparing Duloxetine Versus Placebo in Patients Taking a Nonsteroidal Anti-inflammatory Drug (NSAID) for Knee Pain Due to Osteoarthritis Phase 3
Completed NCT00790790 - A Study in the Treatment of Osteoarthritis Knee Pain Phase 2
Completed NCT00408421 - Duloxetine Versus Placebo for Osteoarthritis Knee Pain Phase 3
Completed NCT03434197 - Safety and Efficacy of SFPP in Knee Osteoarthritis Phase 3
Completed NCT00433290 - Duloxetine vs. Placebo in the Treatment of Osteoarthritis Knee Pain Phase 3