TranScatheter Aortic Valve RepLacement System US Feasibility Trial (SALUS)

This study is currently recruiting participants.
Verified November 2013 by Direct Flow Medical, Inc.
Sponsor:
Information provided by (Responsible Party):
Direct Flow Medical, Inc.
ClinicalTrials.gov Identifier:
NCT01932099
First received: August 20, 2013
Last updated: November 14, 2013
Last verified: November 2013
  Purpose

A study to assess the safety and effectiveness of the Direct Flow Medical aortic valve system. This is for people with severe aortic stenosis who are not well enough to undergo a surgical repair. The delivery of this device is done via the femoral artery.


Condition Intervention Phase
Aortic Valve Stenosis
Device: Transcatheter aortic valve replacement
Phase 2

Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: The Direct Flow Medical TranScatheter Aortic Valve RepLacement System US Feasibility Trial

Resource links provided by NLM:


Further study details as provided by Direct Flow Medical, Inc.:

Primary Outcome Measures:
  • Freedom from all cause mortality/Device success [ Time Frame: 6 months post procedure ] [ Designated as safety issue: Yes ]
    Absence of procedural mortality AND correct positioning of a single prosthetic heart valve into the proper anatomic location AND Intended performance of the prosthetic heart valve (no prosthesis-patient mismatch and mean aortic valve gradient less than 20 mmHg or peak velocity less than 3m/s, AND no moderate or severe prosthetic valve regurgitation.


Secondary Outcome Measures:
  • Early Safety [ Time Frame: 3 months ] [ Designated as safety issue: Yes ]

    Early Safety: as a composite of

    • All-cause mortality
    • All stroke (disabling and non-disabling)
    • Life-threatening bleeding
    • Acute Kidney Injury - Stage 2 or 3 (including renal replacement therapy)
    • Coronary artery obstruction requiring intervention
    • Major vascular complications
    • Valve-related dysfunction requiring repeat procedure (BAV, TAVR, or SAVR)

  • Clinical Efficacy [ Time Frame: 6 months,and annually at 1 to 5 years ] [ Designated as safety issue: No ]

    Clinical Efficacy will be evaluated as a composite of:

    • All-cause mortality
    • All stroke (disabling and non-disabling)
    • Hospitalization for valve-related symptoms or worsening congestive heart failure† (including reporting of days hospitalized)
    • NYHA Class III or IV
    • Prosthetic heart valve dysfunction (mean aortic valve gradient ≥20 mm Hg, EOA ≤0.9-1.1 cm2‡ and/or DVI <0.35, AND/OR moderate or severe prosthetic valve regurgitation*)

  • Time-related Valve Safety [ Time Frame: 30 days, 6 months and annually at 1 to 5 years ] [ Designated as safety issue: Yes ]

    Time-related valve safety will be evaluated as a composite of:

    • Structural valve deterioration:

      • Valve-related dysfunction (mean aortic valve gradient (mean aortic valve gradient ≥20 mm Hg, EOA ≤0.9-1.1 cm2[Depending on body surface area] and/or DVI <0.35, AND/OR moderate or severe prosthetic valve regurgitation [VARC defined])
      • Requiring repeat procedure (TAVR or SAVR)
    • Prosthetic valve endocarditis
    • Prosthetic valve thrombosis
    • Thromboembolic events (e.g., stroke)
    • VARC bleeding, unless clearly unrelated to valve therapy (e.g., trauma)

  • Clinical Endpoints [ Time Frame: 30 days, 6 months and annually at 1 to 5 years. ] [ Designated as safety issue: Yes ]

    Individual Endpoints

    • All-cause mortality
    • Cardiovascular mortality
    • Non-cardiovascular mortality Myocardial Infarction
    • Peri-procedural MI (<72 hours after the index procedure)
    • Spontaneous MI (>72 hours after the index procedure) Neurological Events
    • Stroke

      • Ischemic stroke
      • Hemorrhagic stroke
      • Undetermined
    • Disabling Stroke
    • Non-disabling stroke
    • Transient ischemic attack Bleeding Complications
    • Life-threatening or disabling bleeding
    • Major bleeding
    • Minor bleeding Acute Kidney Injury (AKIN Classification)
    • Stage 1 acute kidney injury
    • Stage 2 acute kidney injury
    • Stage 3 acute kidney injury Vascular Complications
    • Major vascular complications
    • Minor vascular complications
    • Percutaneous closure device failure Prosthetic Valve Dysfunction
    • Prosthetic Aortic Valve Stenosis
    • Prosthesis-Patient Mismatch
    • Prosthetic Aortic Valve Regurgitation


Estimated Enrollment: 30
Study Start Date: August 2013
Estimated Study Completion Date: March 2020
Estimated Primary Completion Date: May 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Single arm feasibility study
Prospective, multi-center, single arm feasibility study. Subjects will include patients with severe aortic valve stenosis who require replacement of their native aortic valve.
Device: Transcatheter aortic valve replacement
Direct Flow Medical Transcatheter Aortic Valve System is indicated for use in aortic stenosis for patients at extreme surgical risk for aortic valve replacement.
Other Name: TAVR

Detailed Description:

The Direct Flow Medical Transcatheter Aortic Valve System is indicated for symptomatic patients who require replacement of their native aortic valve and have a predicted operative mortality or serious morbidity risk of equal or greater 50% at 30 days with surgical aortic valve replacement or are deemed unsuitable for surgery.

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. The patient has severe senile degenerative aortic valve stenosis determined by resting or dobutamine stress echocardiogram and Doppler, or simultaneous pressure recordings at cardiac catheterization defined as: mean gradient >40 mmHg or peak jet velocity >4.0 m/s and an aortic valve area ≤0.8 cm2 or aortic valve area index ≤0.5 cm2/m2.
  2. The patient has moderate to severe symptoms from aortic valve stenosis (NYHA Functional Class ≥III).
  3. The patient must have a predicted risk of operative mortality or serious irreversible morbidity of >50% at 30 days, or be deemed not suitable for surgery for other reasons. This conclusion shall be based on consensus of one cardiologist and two cardiac surgeons at the investigational site after careful consideration of the patient's STS risk score and co-morbidities, and after at least one of the surgeons participating in the decision has personally examined the patient.
  4. The patient been informed of the nature of the study, agrees to its provisions, is willing to comply with protocol-specified follow-up evaluations and has provided written informed consent, approved by the appropriate IRB.

Exclusion Criteria

  1. Left ventricular ejection fraction (LVEF) <20% determined by resting echocardiogram
  2. Patients with an acute MI within 30 days preceding the index procedure.
  3. Any percutaneous coronary or peripheral interventional procedure performed within 30 days prior to the study procedure
  4. Patients with impaired renal function (estimated Glomerular Filtration Rate [eGFR] <20cc/min, calculated from serum creatinine by the Cockcroft-Gault formula)
  5. Patients with a platelet count of <50,000 cells/mm³ or a WBC < 1000 cells/mm³ within 7 days prior to index procedure.
  6. Patients with a history of bleeding diathesis or coagulopathy or patients in whom anti-platelet and/or anticoagulant therapy is contraindicated, or who will refuse transfusion.
  7. Patients who have received any organ transplant or are on a waiting list for any organ transplant.
  8. Patients with known other medical illness (e.g. carcinomas, chronic liver disease, chronic renal disease or chronic end stage pulmonary disease) or known history of substance abuse that may cause non-compliance with the protocol, confound the data interpretation or is associated with a life expectancy of less than one year, or expectation that patient will not improve despite treatment of aortic stenosis.
  9. Patients with known hypersensitivity or contraindication to aspirin, heparin, clopidogrel/ticlopidine, and/or contrast sensitivity that cannot be adequately pre-medicated.
  10. Patients with a history of a stroke or transient ischemic attack (TIA) within the prior 6 months.
  11. Patients with an active gastrointestinal (GI) bleeding within the prior 6 months.
  12. Patients presenting with hemodynamic instability or cardiogenic shock defined by low cardiac output, vasopressor dependence, or mechanical hemodynamic support.
  13. Patients who have a planned treatment with any other investigational device or procedure during the study period, or who are currently participating in an investigational drug or another device trial
  14. Any planned surgical, percutaneous coronary or peripheral procedure to be performed prior to the 30 day follow-up from the TAVR procedure.
  15. Untreated clinically significant coronary artery disease requiring revascularization
  16. Trans-esophageal echocardiography (TEE) is contraindicated
  17. Active endocarditis or sepsis within 6 months prior to the study procedure
  18. Dementia (resulting in either inability to provide informed consent for the trial/procedure, prevents independent lifestyle outside of a chronic care facility, or will fundamentally complicate rehabilitation from the procedure or compliance with follow-up visits)
  19. Congenital bicuspid or unicuspid valve determined by echocardiography
  20. Prior aortic or mitral valve surgery or pre-existing prosthetic heart valve in any position
  21. Native valve annulus diameter is <19mm or >26mm determined by the screening CT scan
  22. Extreme asymmetrical calcification of the native aortic valve determined by the screening CT scan
  23. Echocardiographic evidence of intra-cardiac mass, thrombus, vegetation, or spontaneous echo contrast in the left atrium
  24. >3+ aortic regurgitation, mitral regurgitation or tricuspid regurgitation
  25. Moderate to severe mitral stenosis
  26. Thoracic aortic aneurysm (TAA) or abdominal aortic aneurysm (AAA) >5.0 cm
  27. Presence of an endovascular stent graft for treatment of AAA or TAA 28 Hypertrophic obstructive cardiomyopathy

29. Patients with severe peripheral arterial disease that precludes sheath vascular access (e.g. luminal diameter less than 6.5 mm, severe obstructive calcification or severe tortuosity)

  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01932099

Contacts
Contact: Brian Sheahan 707-576-0420 bsheahan@directflowmedical.com

Locations
United States, California
UC Davis Medical Center Recruiting
Sacramento, California, United States, 95817
Contact: Jeffrey Southhard, MD    916-734-3764    jeffrey.southard@ucdmc.ucdavis.edu   
Contact: W. Douglas Boyd, MD    916-734-7255    douglas.boyd@ucdmc.edu   
Principal Investigator: Jeffrey Southhard, MD         
Principal Investigator: W. Douglas Boyd, MD         
United States, Illinois
Northwestern Memorial Hospital Recruiting
Chicago, Illinois, United States, 60611
Contact: James Flaherty, MD    312-926-6422    jflahert@nmh.org   
Contact: S. Chris Malaisrie, MD    312-695-2517    cmalaisr@nmh.org   
Principal Investigator: James - Flaherty, MD         
Principal Investigator: S. Chris Malaisrie, MD         
United States, Michigan
Henry Ford Hospital Recruiting
Detroit, Michigan, United States, 48202
Contact: William O'Neill, MD    313-916-1878    Woneilli@hfhs.org   
Contact: Gaetano Paone, MD    313-574-2227    Gpaone1@hfhs.org   
Principal Investigator: Wiiliam O'Neill, MD         
Principal Investigator: Gaetano Paone, MD         
United States, Missouri
Washington University Hospital Recruiting
St Louis, Missouri, United States, 63110
Contact: Alan Zajarias, MD    314-454-8475    azajaria@dom.wustl.edu   
Contact: Hersh Maniar, MD    314-362-7431    maniarh@wudosis.wustl.edu   
Principal Investigator: Alan Zajarias, MD         
Principal Investigator: Hersh Maniar, MD         
United States, New York
Columbia Univ. Medical Center Recruiting
New York, New York, United States, 10032
Contact: Susheel Kodali, MD    212-305-7060    sk2427@cloumbia.edu   
Contact: Matt Williams, MD    212-305-9320    ma66@columbia.edu   
Principal Investigator: Susheel Kodali, MD         
Principal Investigator: Matt Williams, MD         
United States, Ohio
Cleveland CLinic Recruiting
Cleveland, Ohio, United States, 44195
Contact: Samir - Kapadia, MD    216-444-6735    kapadis@ccf.org   
Contact: Lars - Svensson, MD    216-445-4813    svens@ccf.org   
Principal Investigator: Samir - Kapadia, MD         
Principal Investigator: Lars - Svensson, MD         
Sponsors and Collaborators
Direct Flow Medical, Inc.
Investigators
Principal Investigator: E. Murat Tuzcu, MD The Cleveland Clinic
Principal Investigator: Patrick M McCarthy, MD Northwestern Memorial Hospital
  More Information

No publications provided

Responsible Party: Direct Flow Medical, Inc.
ClinicalTrials.gov Identifier: NCT01932099     History of Changes
Other Study ID Numbers: IP 011, G12160
Study First Received: August 20, 2013
Last Updated: November 14, 2013
Health Authority: United States: Food and Drug Administration

Keywords provided by Direct Flow Medical, Inc.:
pathological constriction; restricted outflow, stenosis

Additional relevant MeSH terms:
Aortic Valve Stenosis
Constriction, Pathologic
Heart Valve Diseases
Heart Diseases
Cardiovascular Diseases
Ventricular Outflow Obstruction
Pathological Conditions, Anatomical

ClinicalTrials.gov processed this record on April 17, 2014