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Momentum Clinical Trial
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What is the Momentum Clinical Trial

A clinical trial conducted to see if patients hospitalized with decompensated heart failure and are inadequately responding to medication will...

Congestive Heart Failure

CHF is the acronym for congestive heart failure, an often misunderstood disorder in which the heart is...

CancionĀ® System

A medical device that was evaluated for its risks and benefits in patients hospitalized with decompensated heart failure...

New Press Release

Orqis Medical's Cancion System Significantly Increases Cardiac Performance: MOMENTUM Trial Results Presented at ACC 2008

About Orqis Medical

Orqis® Medical Corporation is a privately held medical device company in Orange County, California (USA).  Orqis develops minmally invasive devices that improve cardiac performance through aortic flow therapy. Orqis devices uniquely bridge the treatment gap between medical management and more invasive procedures without ever touching the heart.

Orqis Medical developed continuous aortic flow augmentation (CAFA) as a platform technology to assist the heart’s ability to pump blood.  By augmenting natural blood flow with continuous blood flow in the descending aorta, CAFA changes blood flow dynamics to improve cardiac performance in heart failure patients.  

The percutaneous Cancion® System is commercially available in select markets outside the United StatesThe implantable  Exeleras® System, is currently in development.

The company's novel and proprietary therapeutic devices, and treatment methods, are protected by 14 issued U.S. patents, incorporating over 285 separate claims, and several issued international patents. Orqis® Medical Corporation was founded in 1997.










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Copyright 2007 Orqis Medical Corporation and Orqis International GmbH. Orqis, Cancion, Exeleras, CRS and the heart halo are trademarks of Orqis Medical Corporation in the United States and other countries worldwide. Protected by US and International patents. All rights reserved. CAUTION: Cancion System is Investigational Device. Limited by Federal (United States) Law to Investigational Use. Not Available for Sale in the United States.