3 results
Primary:To determine the degree pain relief 6 months after THA/TKA when screened pre-operative for centralized pain and subsequent treated accordingly for a period of 10 weeks with Duloxetine compared to usual care (no Duloxetine) Secondary:To…
The primary objective of this study is to continue to evaluate the safety and tolerability of LCZ696 in heart failure patients from PARADIGM-HF receiving open-label investigational drug.There are no secondary objectives for this study.
The goal of this study is to compare the initial and long term clinical results and survival of the uncemented and cemented Oxford knee prosthesis.- Does the fixation method affect the knee pain?- Are the radiological criteria for success used for…