Evolut™ EXPAND TAVR II Pivotal Trial

Purpose

Obtain safety and effectiveness data to support indication expansion for the Medtronic TAVR System to include patients with moderate, AS.

Condition

  • Moderate Aortic Valve Stenosis

Eligibility

Eligible Ages
Over 65 Years
Eligible Genders
All
Accepts Healthy Volunteers
No

Inclusion Criteria

o Moderate AS, defined as follows by transthoracic echo (TTE) as assessed by the ECL: - AVA >1.0 cm² and <1.5cm²; or - AVA ≤ 1.0 cm² with AVAI > 0.6cm²/m² if BMI < 30 kg/m²: or - AVA ≤ 1.0 cm² with AVAI > 0.5cm²/m² if BMI ≥ 30 kg/m²: and - Max aortic velocity ≥ 3.0 m/sec. and < 4.0 m/sec. or - Mean aortic gradient ≥ 20mmHg and < 40.0 mmHg Any of the following at-risk features: - Symptoms of AS, defined as: - NYHA ≥ Class II, or - Reduced functional capacity, defined as - 6MWT < 300 meters, or - < 85% of age-sex predicted METs on exercise tolerance testing (ETT) - Documented heart failure event or hospitalization for heart failure within 1 calendar year prior to consent - NT-proBNP ≥ 600 pg/ml (or BNP ≥ 80 pg/ml), or - Persistent AF or Paroxysmal AF episode within 6 months prior to consent, or - Elevated aortic valve calcium score (>1200 AU for females and > 2000 AU for males) as assessed by the MDCT core lab, or - Any of the following by the qualifying TTE as assessed by the ECL: - Global longitudinal strain ≤16% (absolute value), or - E/e' ≥ 14.0 (average of medial and lateral velocities), or - Diastolic dysfunction ≥ Grade II, or - LVEF < 60% - Stroke Volume Index < 35 ml/m² - Anatomically suitable for transfemoral TAVR using the Medtronic Evolut PRO+ or Evolut FX system - The subject and the treating physician agree the subject will return for all required follow-up visits

Exclusion Criteria

  • Age < 65 years - LVEF ≤ 20% by 2-D echo - Class I indication for cardiac surgery - Contraindication for placement of a bioprosthetic valve - Documented history of cardiac amyloidosis

Study Design

Phase
N/A
Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
Medtronic Evolut PRO+, or Evolut FX,TAVR System, & guideline-directed management & therapy (GDMT)
Medtronic Evolut PRO+ TAVR or Evolut FX TAVR Systems, & guideline-directed management & therapy
  • Device: Medtronic Evolut PRO+ TAVR System, or Evolut FX TAVR System, and guideline-directed management and therapy (GDMT)
    Patients will have a Transcatheter Aortic Valve Replacement (TAVR) with either an Evolut PRO+ TAVR, or Evolut FX TAVR, heart valve, and given clinical site-determined guideline-directed management and therapy (GDMT).
No Intervention
Clinical site determined guideline-directed management and therapy (GDMT) alone
Clinical site determined guideline-directed management and therapy (GDMT) alone

Recruiting Locations

University of Alabama at Birmingham (UAB) Hospital
Birmingham, Alabama 35233
Contact:
Mustafa Ahmed, M.D.

More Details

Status
Recruiting
Sponsor
Medtronic Cardiovascular

Study Contact

Hang Nguyen
763-526-2832
hang.t.nguyen@medtronic.com

Detailed Description

Multi-center, international, prospective, randomized study. Subjects will be randomized to either transcatheter aortic valve replacement (TAVR) with the Evolut PRO+ TAVR System, or Evolut FX System, and guideline-directed management (GDMT) or GDMT alone.