11 results
To establish the safety and effectiveness of the Boston Scientific Cardiac Cryoablation System for treatment of symptomatic, drug refractory, recurrent, paroxysmal atrial fibrillation (AF).
Compare 3D biplanar with conventional 2D short axis US guided internal jugular catheterization
This study has been transitioned to CTIS with ID 2024-514073-22-01 check the CTIS register for the current data. To investigate differences in coagulation between (Omniplasma) and FFP in paediatric cardiac patients, who are undergoing cardiac…
The primary objective of this study is to provide a supportive model for optimal coagulation management in the OR and/or ICU to reduce blood loss. This support will be divided into two models to first assess a problem in the coagulation cascade and…
This study has been transitioned to CTIS with ID 2024-515920-35-01 check the CTIS register for the current data. To determine the effect of treatment of postoperative iron deficiency anemia (IDA) with intravenous iron (IVI) on disability 90 days…
The primary objective of the study is survival on a Carmat device at 180 days post-implant* or survival to cardiac transplantation if occurring before 180 days post-implant**. * The beginning of the implant procedure is defined as the start of the…
To demonstrate the safety, performance and effectiveness of the EMPOWER* Modular Pacing System (MPS), as well as the EMPOWER and EMBLEM* Subcutaneous ICD Coordinated System. Additionally, data from this study may be used to support pre-market and…
To describe the perioperative biomarker response in surgical patients with and without a postoperative complication.To construct a preoperative and postoperative prediction model for postoperative complications to improve risk stratification and…
Determine the difference in mitoPO2 in between the cannulated and non-cannulated and the difference in DLS red blood cell velocity (RBV) between the two legs, in patients undergoing a cardiopulmonary bypass (CPB) MICS with standard cannulation.
The primary objective of this study is to assess the effects of CPPF, executed by Haermonics Flush, in comparison with standard care on clinically relevant endpoints, like re-explorations, in a population of cardiac surgery patients that have an…
The primary study objective is the assessment of changes in the stress exhibited by patients using the SAM solution versus those in the control group until the surgical procedure.