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)
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tapentadol | Small molecule | 100 mg | — |
| Subject | Tapentadol | Small molecule | 150 mg | — |
| Subject | Tapentadol | Small molecule | 200 mg | — |
| Subject | Tapentadol | Small molecule | 250 mg | — |