Klinische Studien (Auswahl)

Wir führen zahlreiche klinische Studien, insbesondere zu Herzklappen und Medikamenten durch. Nachfolgend finden Sie eine Auswahl aktueller Forschungsschwerpunkte.

Klinische Studien (Jahr 2014) Studiendesign
AVERT St. Jude
Artificial Valve Endocarditis Reduction Trial: independent, multi-year, multi-center randomized study intended to study the efficacy of silver coating on the valve sewing cuff fabric in reducing the incidence of prosthetic valve endocarditis
Enable I long term
The primary objective of the study is to evaluate the safety and
effectiveness of the Medtronic ATS Enable™ Aortic Bioprosthesis
during long-term follow-up
EASE Studie Enable Aortic Sutureless Bioprosthesis Evaluation, nonrandomized,
prospective, non-interventional multicenter post
market release (PMR) study
Perceval Pivotal
Prospective, multicenter, European, non-randomized. Sutureless,
bovine pericardial stented bioprosthesis
Cavalier Pivotal
Perceval S valve clinical trial for extended CE mark
Freedom Solo
Stentless Heart
Valve Sorin
Biomedica Cardio
Prospective, non-randomized, multicenter trial (CE marked May
2004) Stentless aortic valve made of bovine pericardium
FOUNDATION Assessing standard of care and clinical outcomes using the
Edwards intuity valve system in a European multicenter, active,
post-market surveillance study. Prospective, single arm, multicenter
SURTAVI SURTAVI Surgical Replacement and Transcatheter Aortic Valve
Implantation. Subject will be randomized on a 1:1 basis to either
transcatheter aortic valve implant (TAVI) with the Medtronic
CoreValve® System (MCS) or to surgical aortic valve replacement
Perigon PERIcardial SurGical Aortic Valve ReplacemeNt Pivotal Trial
Cathar Comparison of antithrombotic treatments after aortic valve
replacement. Rivaroxaban: A new Antithrombotic Treatment for
Patients with Mechanical Prostesic Aortic Heart Valve
Swiss-TAVIRegistry Prospective, National, Multi-Center Registry of Patients Undergoing Transcatheter Aortic Valve Implantation
SAVI 2 Symetis ACURATE TA™ Valve Implantation Register 2:SAVI 2
CardioGard A study to collect additional information related to the safety and
performance of the CardioGard cannula
eMesh A multicenter, randomized study of external saphenous vein
support using eSVS Mesh in CABAG Surgery
Metabolomics Metabolic factors positively associated with the non-development of
coronary artery disease
EAGLE Registry Endurant for Challenging Anatomy: Global Experience Registry
Thoraflex™ Hybrid To monitor the post-market clinical safety and performance of the Vascutek Thoraflex™ Hybrid Graft in patients requiring a “frozen Elephant Trunk” procedure to replace the aortic arch and repair aneurysm and/or dissection of the descending aorta in a single surgical procedure. All patients implanted with a Vascutek Thoraflex™ Hybrid Device and who consent to the use of their data will be included in the registry.