drugset / Trial / NCT01631513

An Open-label Evaluation of Tapentadol Extended Release (ER) in Participants With Moderate to Severe Chronic Pain After Conversion From Hydrocodone, Oxycodone Controlled Release (CR), and/or Morphine Sustained Release (SR)

NCT01631513

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate tapentadol Extended Release (ER) in the treatment of moderate to severe chronic pain in participants with a diagnosis of chronic low back pain (LBP) or osteoarthritis (OA) of the hip or knee after conversion from hydrocodone, oxycodone Controlled Release (CR), and/or morphine Sustained Release (SR).

Timeline

Start
2012-08
Primary completion
2012-08
Completion
2013-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Tapentadol Small molecule 100 mg
Subject Tapentadol Small molecule 150 mg
Subject Tapentadol Small molecule 200 mg
Subject Tapentadol Small molecule 250 mg