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REPRISE II: REpositionable Percutaneous Replacement of Stenotic Aortic Valve Through Implantation of Lotus™ Valve System

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01627691
Recruitment Status : Active, not recruiting
First Posted : June 26, 2012
Last Update Posted : May 24, 2018
Information provided by (Responsible Party):
Boston Scientific Corporation

Brief Summary:
The purpose of this study is to evaluate the safety and performance of the Lotus™ Valve System for transcatheter aortic valve replacement (TAVR) in symptomatic subjects with severe calcific aortic stenosis who are considered high risk for surgical valve replacement.

Condition or disease Intervention/treatment Phase
Transcatheter Aortic Valve Replacement Device: Lotus Valve System Not Applicable

Detailed Description:
The REPRISE II clinical study is a prospective, single-arm, multicenter study designed to evaluate the safety and performance of the Lotus Valve System for TAVR in symptomatic subjects who have severe calcific aortic valve stenosis and who are at high risk for surgical aortic valve replacement (SAVR).

Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 250 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: REPRISE II: REpositionable Percutaneous Replacement of Stenotic Aortic Valve Through Implantation of Lotus™ Valve System - Evaluation of Safety and Performance
Actual Study Start Date : October 8, 2012
Actual Primary Completion Date : May 30, 2014
Estimated Study Completion Date : June 13, 2019

Arm Intervention/treatment
Experimental: Lotus Valve System
Patients enrolled will receive the Lotus Valve.
Device: Lotus Valve System
  • bioprosthetic bovine pericardial aortic valve
  • delivery system

Primary Outcome Measures :
  1. Primary Device Performance Endpoint: Mean aortic valve pressure gradient at 30 days post implant procedure [ Time Frame: 30 days ]
    Mean aortic valve pressure gradient at 30 days post implant procedure as measured by echocardiography and assessed by an independent core laboratory.

  2. Primary Safety Endpoint: All-cause mortality at 30 days post implant procedure [ Time Frame: 30 days ]
    All-cause mortality at 30 days post implant procedure

Information from the National Library of Medicine

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Ages Eligible for Study:   70 Years and older   (Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Subject is ≥70 years of age
  • Subject has documented calcific native aortic valve stenosis
  • Subject has a documented aortic annulus size between ≥19 and ≤27 mm based on pre-procedure diagnostic imaging
  • Symptomatic aortic valve stenosis with NYHA Functional Class ≥ II
  • Subject is considered high risk for surgical valve replacement
  • Heart team assessment that the subject is likely to benefit from valve replacement.
  • Subject (or legal representative) understands the study requirements and the treatment procedures, and provides written informed consent.
  • Subject, family member, and/or legal representative agree(s) and subject is capable of returning to the study hospital for all required scheduled follow up visits.

Exclusion Criteria:

  • Subject has a congenital unicuspid or bicuspid aortic valve.
  • Subject with an acute myocardial infarction within 30 days of the index procedure
  • Subject has had a cerebrovascular accident or transient ischemic attack within the past 6 months, or has any permanent neurologic defect prior to study enrollment.
  • Subject is on dialysis or has serum creatinine level >3.0 mg/dL or 265 µmol/L.
  • Subject has a pre-existing prosthetic heart valve (aortic or mitral) or a prosthetic ring in any position.
  • subject cannot have more than moderate mitral, aortic or tricuspid regurgitation
  • Subject has a need for emergency surgery for any reason.
  • Subject has a history of endocarditis within 12 months of index procedure or evidence of an active systemic infection or sepsis.
  • Subject has echocardiographic evidence of intra-cardiac mass, thrombus or vegetation.
  • Subject has low Hgb, platelet count or >700,000 cells/mm3, or low white blood cell count.
  • Subject requires chronic anticoagulation therapy and cannot tolerate concomitant therapy with either aspirin or clopidogrel/ticlopidine
  • Subject has active peptic ulcer disease or gastrointestinal bleed within the past 3 months, other bleeding diathesis or coagulopathy or will refuse transfusions.
  • Subject has known hypersensitivity to contrast agents that cannot be adequately pre-medicated, or has known hypersensitivity to aspirin, all thienopyridines, heparin, nickel, tantalum, titanium, or polyurethanes.
  • Subject has a life expectancy of less than 12 months due to non-cardiac, co-morbid conditions based on the assessment of the investigator at the time of enrollment.
  • Subject has hypertrophic obstructive cardiomyopathy.
  • Subject has any therapeutic invasive cardiac procedure within 30 days prior to the index procedure (except for pacemaker implantation which is allowed).
  • Subject has untreated coronary artery disease.
  • Subject has documented left ventricular ejection fraction <30%.
  • Subject is in cardiogenic shock or has hemodynamic instability requiring inotropic support or mechanical support devices.
  • Subject has severe peripheral vascular disease or symptomatic carotid or vertebral disease.
  • Narrow Femoral artery lumen precludes the use of either Lotus device size, or severe iliofemoral tortuosity or calcification that would prevent safe placement of the introducer sheath.
  • Current problems with substance abuse (e.g., alcohol, etc.).
  • Subject is participating in another investigational drug or device study that has not reached its primary endpoint.
  • Patient has preexisting untreated conduction system disorder that requires new pacemaker implantation.

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01627691

Royal Adelaide Hospital
Adelaide, Australia
Prince Charles Hospital
Brisbane, Australia
Monash Medical Center
Melbourne, Australia
St. Vincent's Hospital
Melbourne, Australia
Hôpital Cardiologique CHRU de Lille
Lille, France
Hôpital Cardiologique de Lyon
Lyon, France
Institut Cardiovasculaire Paris Sud
Paris, France
Centre Hôpital Universitaire Rangueil
Toulouse, France
Clinique Pasteur
Toulouse, France
Deutsches Herzzentrum München
München, Germany
Helios Klinikum Siegburg
Siegburg, Germany
Ospedale Ferrarotto
Catania, Italy
Erasmus MC - Thorax Center
Rotterdam, Netherlands
Hospital Clinico San Carlos
Madrid, Spain
University Hospital of Lund
Lund, Sweden
INSELSPITAL - Universitätsspital Bern
Bern, Switzerland
United Kingdom
Royal Victoria Hospital
Belfast, United Kingdom
Royal Sussex County Hospital
Brighton, United Kingdom
The General Infirmary
Leeds, United Kingdom
Guys and St. Thomas NHS Foundation Trust
London, United Kingdom
Sponsors and Collaborators
Boston Scientific Corporation
Principal Investigator: Ian Meredith, Professor Monash Medical Centre

Publications automatically indexed to this study by Identifier (NCT Number):
Responsible Party: Boston Scientific Corporation Identifier: NCT01627691     History of Changes
Other Study ID Numbers: TP3687
TP3687 ( Other Identifier: Boston Scientific )
First Posted: June 26, 2012    Key Record Dates
Last Update Posted: May 24, 2018
Last Verified: May 2018
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No