3 results
The primary objective of this study is to evaluate the efficacy of TDF plus Peginterferon *-2a (PEG) combination therapy for 48 weeks versus standard of care TDF monotherapy or PEG monotherapy for 48 weeks in non-cirrhotic CHB subjects as determined…
The primary objective is to investigate whether pharmacological conditioning with S(+)-ketamine compared to pharmacological conditioning with placebo medication reduces pain sensitivity in patients with FMS.
The aim of the FAST OCT study is to define the correlation between 3D-angio-based FFR values and OCT findings in a pre- and post-PCI setting in patients with non-ST segment elevation acute coronary syndromes (NST-ACS). The results will be used to…