3 results
Approved WMOCompleted
The primary objective of this study is to investigate the safety and feasibility of implanting a WATCHMAN Device in a hybrid setup for AF ablation.
Approved WMOCompleted
To evaluate the safety of the EndoArt* implanted in subjects suffering from corneal edema.
Approved WMOCompleted
Main objective: to determine the effect, defined as the percentage of patients that show a clinical relevant improvement on the severity of complaints of nocturnal sialorrhea, of oral glycopyrroniumbromide in comparison with placebo in psychiatric…