Last updated on January 2009

Dynamic Annuloplasty System With Activation for the Treatment of Mitral Regurgitation

Are you eligible to participate in this study?

You may be eligible for this study if you meet the following criteria:

• Conditions: Mitral Valve Regurgitation
• Age: Between 18 - 100 Years
• Gender: Male or Female

• Other:
  This patient requires mitral valve repair with or without concomitant procedures such
  as coronary artery bypass or another valve reconstruction or replacement.
  This patient has been diagnosed with a diseased natural valve, based on
  echocardiography and is a candidate for mitral valve repair.
  This patient is in satisfactory condition, based on the physical exam and
  investigator's experience, to be an average or better operative risk. (i.e., likely
  to survive one year postoperatively).
  This patient is geographically stable and willing to return to the implant center for
  follow-up visits.
  This patient has been adequately informed of his/her participation in the clinical
  tudy, and of what will be required of him/her, in order to comply with the protocol.
  

You may not be eligible for this study if the following are true:

• This patient is less than eighteen (18) years of age.
  This patient has a non-cardiac major or progressive disease, which in the
  investigator's experience produces an unacceptable increased risk to the patient, or
  results in a life expectancy of less than twelve months.
  This patient has an ejection fraction < 30%.
  This patient has a heavily calcified annulus or leaflets.
  This patient presents with active endocarditis or has had active endocarditis in the
  last 3 months.
  This patient is pregnant (urine HCG test result positive) or lactating.
  This patient is an intravenous drug abuser or alcohol abuser.
  This patient has a previously implanted prosthetic mitral valve.
  This patient requires mitral valve replacement.
  This patient has a creatinine level > 2.0 mg/dl
  This patient has had congestive heart failure within the past 6 months requiring
  urgical treatment.
  This patient has had a coronary artery ischemic event within the past 6 months.
  This patient has a known life threatening, non-cardiac disease that will limit the
  patient's life expectancy to less than one year.
  This patient is unable to take Coumadin.
  This patient has a known untreatable allergy to contrast media or nickel.
  This patient has had a cerebral vascular event within the past 6 months.
  This patient is a prisoner (U.S.A. Only).
  This patient is participating in concomitant research studies of investigational
  products.
  This patient will not agree to return to the implant center for the required number
  of follow-up visits or is geographically unavailable for follow-up.