Symphony: The Implantable Counter Pulsation Device (CPD) Safety and Feasibility Trial

This study is currently recruiting participants. (see Contacts and Locations)
Verified May 2013 by Abiomed Inc.
Sponsor:
Information provided by (Responsible Party):
Abiomed Inc.
ClinicalTrials.gov Identifier:
NCT01543022
First received: February 27, 2012
Last updated: May 1, 2013
Last verified: May 2013

February 27, 2012
May 1, 2013
November 2011
December 2013   (final data collection date for primary outcome measure)
Death, Stroke or Transient Ischemic Attack (TIA), Limb Ischemia requiring surgical intervention [ Time Frame: hospital discharge or 30 days of support, whichever is longer ] [ Designated as safety issue: Yes ]
The trial will primarily look at patient safety defined as proportion of composite Major Adverse Events (MAE) up to hospital discharge or 30 days of CPD support, whichever is longer.
Same as current
Complete list of historical versions of study NCT01543022 on ClinicalTrials.gov Archive Site
Not Provided
Not Provided
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Symphony: The Implantable Counter Pulsation Device (CPD) Safety and Feasibility Trial
First in Man Study - a Prospective, Multicenter, Single Arm Trial to Investigate the Safety and Feasibility of the Symphony Device

The Counter Pulsation Device (CPD) System 'Symphony' is intended to provide counter pulsation therapy for up to thirty (30) days to patients with chronic heart failure who have persistent worsening of their condition despite optimal medical therapy. Patients will be in New York Heart Association (NYHA) Class IIIb or IV heart failure and have exhausted all medical or surgical options.

Not Provided
Interventional
Phase 1
Phase 2
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Chronic Heart Failure
  • Device: Symphony
    The Symphony system has been developed for superficial implantation without the need to enter the chest. It allows for complete patient mobility and provides counter pulsation therapy for up to 30 days in hospitalized patients.
  • Procedure: The operative approach is limited to an infraclavicular incision similar to that used for placement of a pacemaker
    The vascular graft is surgically attached (anastomosed) to the subclavian artery. The symphony device is implanted into a pocket below the pectoralis muscle on the anterior chest and attached to the graft. The driveline is tunneled out through the skin and attached to the drive console.
Experimental: Symphony system
Interventions:
  • Device: Symphony
  • Procedure: The operative approach is limited to an infraclavicular incision similar to that used for placement of a pacemaker
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
10
June 2014
December 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. New York Heart Association Class IIIB or IV heart failure despite optimal medical therapy, including ACE inhibitors, beta blockers, IV diuretics and pressors
  2. Left Ventricular Ejection Fraction < 40%.
  3. Patient is not a candidate for conventional catheter-based or surgical intervention such as valve intervention or coronary artery bypass surgery.
  4. Patient is not currently a candidate for heart transplantation or placement of a left ventricular assist device (LVAD) as bridge to heart transplantation due to co-morbidities. Patients may become a candidate for these options if they have improvement on the device due to improved cardiac output.
  5. Patients have exhausted all approved surgical and medical therapies as determined by a heart failure cardiologist and a surgeon with expertise in heart failure.
  6. Patient has been evaluated by a multi-disciplinary research team and felt to be a suitable candidate for a research study. The final decision regarding the patient's candidacy for research will remain with the attending cardiologist and heart surgeon.
  7. Improved hemodynamics on device support will allow for potential for physical rehabilitation.
  8. Signed Informed Consent, or oral informed consent with written confirmation by uninvolved third party
  9. Age of subject at least 19 years

Exclusion Criteria:

  1. High likelihood of death during the current hospitalization (as judged by the attending physician) and condition other than heart failure that would limit survival to less than two years.
  2. Require mechanical ventilation.
  3. Failure to wean from IABP, Impella, ECMO or other mode of circulatory support.
  4. Complex arrhythmias that negatively impact the effectiveness of counter pulsation.
  5. Dependency on high dose inotropes.
  6. Cerebrovascular accident or TIA within the previous 3 months.
  7. Contraindication to anticoagulation medication such as Heparin, Coumadin, Aspirin and Plavix.
  8. Presence of hypercoaguable state or history of idiopathic venous or arterial thrombosis.
  9. Severe calcification in the target vessel that will preclude insertion of the Symphony device.
  10. Moderate to severe aortic insufficiency (2+ or more).
  11. Ongoing systemic infection defined as two of the following:

    • WBC > 12,500
    • positive blood culture
    • fever
  12. Abnormal pre-albumin (< 13mg/dL), or albumin (< 3.0 mg/dl)
  13. A cardiac rhythm that cannot be used to trigger the CPD (sinus rhythm, ventricular or atrial pacing, A-V pacing).
  14. Abnormal bilateral carotid Doppler or CT exam define as > 50% stenosis.
  15. Subclavian artery internal diameter of < 7 mm on Doppler study or CT exam.
  16. Ability to ambulate < 200 metres on a 6 minute walk test.
  17. Any aortic aneurysmal disease.
  18. Active documented HIT.
  19. Presence of mechanical heart valve.
  20. Moderate to severe RV failure.
  21. Severe tricuspid regurgitation.
  22. History of major psychiatric illness.
  23. End-organ dysfunction including:

    • renal failure defined as serum Cr > 2.5 mg/dl,
    • liver dysfunction defined as bilirubin 2X normal, or elevated INR with no anticoagulation,
    • respiratory failure defined as FEV1 < 50% predicted.
  24. Chest X-ray to rule out pulmonary pathology that increases the risk of need for treatment prior to device implant.
  25. BMI > 40 kg/ m2.
  26. Active participation in another clinical trial that may interfere with this trial.
Both
19 Years and older
No
Contact: Carol Loring 781-646-1595 cloring@abiomed.com
Canada
 
NCT01543022
184916
Yes
Abiomed Inc.
Abiomed Inc.
Not Provided
Not Provided
Abiomed Inc.
May 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP