3 results
Approved WMOPending
To evaluate the efficacy of Arnica om postoperative outcome after upper blepharoplasty.
Approved WMOCompleted
The primary objective of the study is to evaluate the safety and tolerability of the Occlutech® AFR device by assessing the incidence of SADEs in the 3 months following implantation. Secondary objectives are related to safety and efficacy:• To…
Approved WMOWill not start
The objective of this study is to investigate whether an interatrial shunt device is superior to sham procedure in prevention of: (1) incidence of and time to cardiovascular mortality through 12-24 months; (2) incidence of and time to heart…