Sorin Group Announces The First Inclusion In The Clepsydra Clinical Study In The US

(MIL:) announced today the first inclusion of a patient in the Clepsydra clinical trial. The study will investigate the sensitivity to changes in status of PhD™, a unique using the dual of and to monitor patient’s breathing and activity levels every day. The algorithm aims to provide physicians with both trends and indicators in order to highlight sustained changes in overall health status that could relate to (HF) evolution.

PhD™ is available in the Paradym™ family of Implantable Cardioverter Defibrillators (ICD) in Europe and under in Implantable Defibrillators (CRT-D) in Europe and US.

According to the (AHA) and the European Society of Cardiology (ESC) Guidelines, currently affects about 5 million Americans and 15 million people in the 35 countries under the auspices of the ESC.

is the most common Medicare diagnosis-related group ( diagnosis), and more are spent for the diagnosis and treatment of HF than for any other diagnosis. In Europe, HF accounts for about 2% of on health.

As the severity of HF can fluctuate and adjusted to improve the patient’s condition, it is important to monitor recognised indicators of to prevent the patient being hospitalized. PhD™ measures activity workload and ventilation at rest and exercise, which are two key measurements to indicate that a patient’s condition is progressing. The Clepsydra study will test the PhD™ algorithm that is designed to give of sustained deterioration. Advanced warning at follow-up could give physicians time to intervene in the patient’s treatment to avoid the costs and patient burden associated with .

The Clepsydra study, will evaluate PhD™ in 550 patients to be enrolled in the US and Europe. Patients will be closely monitored over a minimum of 13 months by hospital visits and by telephone checks.

The first implant was performed by Andrew J. Kaplan, MD, cardiac electrophysiologist with CVAM, CardioVascular Associates of Mesa, at Mountain Vista Medical Center in Mesa, Arizona, USA.

Dr. Kaplan noted, “Tracking and managing progression in our patients is complex and time consuming. The Clepsydra study should help us better predict and intervene earlier in the process through evaluation of the data collected by the PhD™ sensor-based function. The implantation in our first patient was smooth and the device performed well”.

“Our vision is to provide new and innovative tools to physicians and relieve the burden of for all stakeholders. Monitoring of the patient physiological status (PhD) is an important step to giving physicians an accurate guide to optimizing therapy and avoid costly hospitalizations. The Clepsydra study highlights ’s commitment to backing our leading technologies with large scale clinical justification”, said Stefano Di Lullo, President of Cardiac Rhythm Management (CRM) Business Unit.

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