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Clinical Trial Summary

The primary purpose of this study is to determine if duloxetine reduces pain severity in patients with osteoarthritis knee pain.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00433290
Study type Interventional
Source Eli Lilly and Company
Contact
Status Completed
Phase Phase 3
Start date February 2007
Completion date May 2008

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 NCT00945945 - A Study of Duloxetine in Patients With Osteoarthritis Knee Pain Phase 3
Completed NCT03434197 - Safety and Efficacy of SFPP in Knee Osteoarthritis Phase 3