CardioMEMS HF System Post Approval Study



Status:Active, not recruiting
Conditions:Cardiology
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - Any
Updated:10/21/2017
Start Date:January 2015
End Date:June 2020

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The purpose of the CardioMEMS HF System Post Approval Study (PAS) is to evaluate the use of
the CardioMEMS HF System in patients with NYHA class III heart failure in a commercial
setting.


Inclusion Criteria:

- Diagnosis of NYHA class III heart failure

- At least 1 heart failure hospitalization within previous 12 months

- Patients with reduced LVEF heart failure should be receiving a beta blocker for 3
months and an ACE-I or ARB for one month unless in the investigator's opinion, the
patient is intolerant to beta blockers, ACE-I or ARB

- BMI ≤ 35. Patients with BMI >35 will require their chest circumference to be measured
at the axillary level. If > 65 inches the patient will not be eligible for the study.

- Pulmonary artery branch diameter ≥ 7mm - (implant target artery - assessed during the
right heart catheterization)

Exclusion Criteria:

- Active infection

- History of recurrent (> 1) pulmonary embolism or deep vein thrombosis

- Inability to tolerate a right heart catheterization

- A major cardiovascular event (e.g., myocardial infarction, open heart surgery, stroke,
etc.) within previous 2 months

- Cardiac resynchronization device (CRT) implanted within previous 3 months

- Glomerular Filtration Rate (GFR) < 25 ml/min (obtained within 2 weeks of implant) who
are non-responsive to diuretic therapy or who are on chronic renal dialysis

- Congenital heart disease or mechanical right heart valve

- Likely to undergo heart transplantation or VAD within the next 6 months

- Known coagulation disorders

- Hypersensitivity or allergy to aspirin, and/or clopidogrel
We found this trial at
1
site
Morgantown, West Virginia 26505
Principal Investigator: Robert Hull, MD
Phone: 304-293-0615
?
mi
from
Morgantown, WV
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