Post TAVI Coronary REVASCularisation Guided by Myocardial Perfusion Imaging: a Prospective Open Label Pilot Study: The REVASC-TAVI Study (REVASC-TAVI)
Primary Purpose
Severe and Symptomatic Aortic Stenosis, Stable Coronary Disease
Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
TAVI procedure
Sponsored by
About this trial
This is an interventional treatment trial for Severe and Symptomatic Aortic Stenosis focused on measuring TAVI, Aortic stenosis, Coronary artery disease, Coronary angiography, Percutaneous Coronary Intervention, Myocardial ischemia, SPECT, Coronary revascularization
Eligibility Criteria
Inclusion Criteria:
- Patients older than 18 years
- Severe and symptomatic aortic stenosis defined as a median trans-valvular gradient higher than 40 mmHg and an aortic valve area of less than 1.0 cm2 or 0,6 cm2/m2 on echocardiography associated to significant CAD defined by ≥1 stenosis of ≥70% in a major epicardial coronary artery or ≥50% for left main
- Patients is not candidate for surgical aortic valve replacement after the multidisciplinary heart team decision.
Exclusion Criteria:
- Recent acute coronary syndrome (within 30 days before randomization),
- Unprotected left main disease
- Critical stenosis (>90%) of Left Anterior Descending artery (LAD),
- Significant angina (CCS class more than 2)
- Active bleeding,
- Contraindication for tomographic technetium-99 assessment or dipyridamole injection
- Previous enrollment in a other study
- Impossibly to obtain consent
Sites / Locations
- Montpellier University Hospital
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Interventional Arm
Arm Description
Outcomes
Primary Outcome Measures
The primary endpoint is a composite of all cause of death
Mortality is defined as death due to any cause, the exact nature and date of which will be recorded. All deaths will be considered cardiovascular-related unless there is documentation to the contrary.
The primary endpoint is a composite of stroke
The primary endpoint is a composite of major bleeding
Major bleedings are defined by ≥2 BARC classification.
The primary endpoint is a composite of major vascular complication
Access site complications is defined in accordance with the Valve Academic Research Consortium (VARC) guidelines.
The primary endpoint is a composite of periprocedural myocardial infarction
Perprocedural myocardial infarction is defined by 5-fold increased of basal troponin level associated to angina or ECG changes
The primary endpoint is a composite of hospitalization for cardiac cause.
Secondary Outcome Measures
Post-TAVI mortality
Major adverse cardiovascular or cerebrovascular event (MACCE)
Acute coronary syndrome (ACS)
Acute myocardial infarction (MI)
Rate of stroke
Repeat revascularization by either PCI or CABG
Hospitalization for heart failure or for non cardiovascular causes
Duration of hospital stay
Quality of life by Kansas city cardiomyopathy questionnaire
Per-procedural complications
ventricular fibrillation (VF), ventricular tachycardia (VT) requiring cardioversion, cardiopulmonary arrest requiring cardiopulmonary resuscitation (CPR) and/or assisted mechanical respiratory support
percentage of pacemaker after implantation of the valve
Bleeding complications according to the BARC classification
Severe VARC Access Site Complications (Safety Issue at 1 and 6 months)
Full Information
NCT ID
NCT02797158
First Posted
May 30, 2016
Last Updated
July 23, 2019
Sponsor
University Hospital, Montpellier
1. Study Identification
Unique Protocol Identification Number
NCT02797158
Brief Title
Post TAVI Coronary REVASCularisation Guided by Myocardial Perfusion Imaging: a Prospective Open Label Pilot Study: The REVASC-TAVI Study
Acronym
REVASC-TAVI
Study Type
Interventional
2. Study Status
Record Verification Date
May 2019
Overall Recruitment Status
Completed
Study Start Date
June 23, 2016 (Actual)
Primary Completion Date
July 15, 2019 (Actual)
Study Completion Date
July 15, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Montpellier
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Evaluation of a strategy of selected revascularization guided on myocardial ischemia detection after the TAVI procedure by using single photon emission computed tomography (SPECT) myocardial perfusion imaging.
Detailed Description
Background: Percutaneous coronary intervention (PCI) is usually proposed to patients with aortic stenosis (AS) before TransAortic Valve Implantation (TAVI) when significant coronary stenosis is detected on preprocedural coronary angiography. However, the benefit of a systematic revascularisation is unknown and may have specific complications in elderly and frail patients.
Aims: The investigators proposed a strategy of selected revascularization guided on myocardial ischemia detection after the TAVI procedure by using single photon emission computed tomography (SPECT) myocardial perfusion imaging.
Methods: This prospective open label clinical trial will include 71 consecutive patients with significant coronary artery disease (CAD) defined by one or more significant coronary stenosis in patients admitted for TAVI. Myocardial SPECT imaging will be performed in all patients at 1-month follow-up after the TAVI procedure. Targeted PCI will be performed only in patients with significant related ischemia (> 10 % myocardial perfusion defect).
The primary outcome criterion is a composite criterion of feasibility and safety including all causes of death, stroke, major bleedings, major vascular complications, per procedural myocardial infarction, coronary revascularization or rehospitalisation for cardiac cause at 6 month follow-up.
Hypothesis: An alternative management of CAD guided by significant myocardial ischemia detection after TAVI could reduce the risk of unnecessary revascularization, the complications and the costs inherent to these procedures and a phase II trial is requiring to the evaluate this innovative and less invasive strategy.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Severe and Symptomatic Aortic Stenosis, Stable Coronary Disease
Keywords
TAVI, Aortic stenosis, Coronary artery disease, Coronary angiography, Percutaneous Coronary Intervention, Myocardial ischemia, SPECT, Coronary revascularization
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
71 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Interventional Arm
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
TAVI procedure
Intervention Description
Targeted and selected revascularization guided on myocardial ischemia detection after the TAVI procedure by using single photon emission computed tomography (SPECT) myocardial perfusion imaging.
Primary Outcome Measure Information:
Title
The primary endpoint is a composite of all cause of death
Description
Mortality is defined as death due to any cause, the exact nature and date of which will be recorded. All deaths will be considered cardiovascular-related unless there is documentation to the contrary.
Time Frame
6 months
Title
The primary endpoint is a composite of stroke
Time Frame
6 months
Title
The primary endpoint is a composite of major bleeding
Description
Major bleedings are defined by ≥2 BARC classification.
Time Frame
6 months
Title
The primary endpoint is a composite of major vascular complication
Description
Access site complications is defined in accordance with the Valve Academic Research Consortium (VARC) guidelines.
Time Frame
6 months
Title
The primary endpoint is a composite of periprocedural myocardial infarction
Description
Perprocedural myocardial infarction is defined by 5-fold increased of basal troponin level associated to angina or ECG changes
Time Frame
6 months
Title
The primary endpoint is a composite of hospitalization for cardiac cause.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Post-TAVI mortality
Time Frame
1 and 6 months
Title
Major adverse cardiovascular or cerebrovascular event (MACCE)
Time Frame
1 and 6 months
Title
Acute coronary syndrome (ACS)
Time Frame
1 and 6 months
Title
Acute myocardial infarction (MI)
Time Frame
1 and 6 months
Title
Rate of stroke
Time Frame
1 and 6 months
Title
Repeat revascularization by either PCI or CABG
Time Frame
1 and 6 months
Title
Hospitalization for heart failure or for non cardiovascular causes
Time Frame
1 and 6 months
Title
Duration of hospital stay
Time Frame
1 and 6 months
Title
Quality of life by Kansas city cardiomyopathy questionnaire
Time Frame
1 and 6 months
Title
Per-procedural complications
Description
ventricular fibrillation (VF), ventricular tachycardia (VT) requiring cardioversion, cardiopulmonary arrest requiring cardiopulmonary resuscitation (CPR) and/or assisted mechanical respiratory support
Time Frame
1 and 6 months
Title
percentage of pacemaker after implantation of the valve
Time Frame
1 and 6 months
Title
Bleeding complications according to the BARC classification
Time Frame
1 and 6 months
Title
Severe VARC Access Site Complications (Safety Issue at 1 and 6 months)
Time Frame
1 and 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients older than 18 years
Severe and symptomatic aortic stenosis defined as a median trans-valvular gradient higher than 40 mmHg and an aortic valve area of less than 1.0 cm2 or 0,6 cm2/m2 on echocardiography associated to significant CAD defined by ≥1 stenosis of ≥70% in a major epicardial coronary artery or ≥50% for left main
Patients is not candidate for surgical aortic valve replacement after the multidisciplinary heart team decision.
Exclusion Criteria:
Recent acute coronary syndrome (within 30 days before randomization),
Unprotected left main disease
Critical stenosis (>90%) of Left Anterior Descending artery (LAD),
Significant angina (CCS class more than 2)
Active bleeding,
Contraindication for tomographic technetium-99 assessment or dipyridamole injection
Previous enrollment in a other study
Impossibly to obtain consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Florence LECLERCQ, PU PH
Organizational Affiliation
Montpellier University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Montpellier University Hospital
City
Montpellier
ZIP/Postal Code
34295
Country
France
12. IPD Sharing Statement
Learn more about this trial
Post TAVI Coronary REVASCularisation Guided by Myocardial Perfusion Imaging: a Prospective Open Label Pilot Study: The REVASC-TAVI Study
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