Congestive Heart Failure Clinical Trial
Official title:
The V-Wave Shunt For 'Left Atrial Decompression' In Patients With Advanced Chronic Heart Failure: FIM Safety and Feasibility Study
The V-Wave atrial-septal shunt implant is intended for the reduction of elevated left atrial filling pressures ('Left Atrial Decompression') in chronic, New York Heart Association (NYHA) class III -IV, Heart Failure (HF) patients. This is a First In Man (FIM) study, aimed to enable a first evaluation of the safety and performance of the V-Wave shunt implant when implanted in Chronic Heart Failure patients. Prospective, open label, single-arm study with intra-patient comparisons (i.e. subjects' status will be compared to their pre-implant (baseline) status.
V-Wave Ltd, an Israeli based medical device company, has developed the V-Wave atrial-septal
shunt, a permanent implant indicated for Heart Failure (HF) patients with elevated Left
Atrial filling Pressures (LAP). The V-Wave shunt, developed by V-Wave Ltd, has been designed
specifically to meet the needs of an interatrial shunt and thus represents a dedicated
device, to be implanted percutaneously in the interatrial septum creating an interatrial
communication.
This study aims to enable a first evaluation of the safety and performance of the V-Wave
shunt implant when implanted in Heart Failure patients with elevated LAP. Study endpoints
were then chosen to portray both safety (device related Major Adverse Cardiac And
Neurological Events) as well as preliminary performance as assessed by a well characterized
measure (e.g., LAP which is known to be associated with the general state of the disease and
most importantly left ventricular ejection fraction and cardiac function in general).
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