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A Prospective Study of Fractional Flow Reserve Assessment of Intermediate Coronary Stenoses in Severe Aortic Stenosis

Primary Purpose

Coronary Artery Stenoses, Aortic Stenosis

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Volcano iFR/FFR Verrata Plus coronary pressure/flow wire
Sponsored by
The Cleveland Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Coronary Artery Stenoses focused on measuring Coronary Artery Stenoses, Aortic Stenosis

Eligibility Criteria

20 Years - 110 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • All patients who have coronary stenoses between 40-70% severity and who have severe aortic stenosis undergoing TAVR work-up.

Exclusion Criteria:

  • Patients with documented intraprocedural hemodynamic instability, shock, or major adverse event (myocardial infarction, aortic rupture/dissection, stroke, left ventricular perforation, cardiac arrest).
  • Contraindication to adenosine, presence of cardiogenic shock, presence of acute coronary syndrome.

Sites / Locations

  • The Cleveland Clinic

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

FFR/iFR arm

Arm Description

Volcano iFR/FFR Verrata Plus coronary pressure/flow wire

Outcomes

Primary Outcome Measures

FFR Values Prior to Transcatheter Aortic Valve Replacement
Hemodynamic significance of a coronary stenosis by measuring FFR immediately prior to TAVR
FFR Values During the Transcatheter Aortic Valve Replacement (TAVR)
Hemodynamic significance of a coronary stenosis by measuring FFR immediately after TAVR

Secondary Outcome Measures

Full Information

First Posted
February 6, 2018
Last Updated
December 13, 2022
Sponsor
The Cleveland Clinic
Collaborators
Volcano Corporation
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1. Study Identification

Unique Protocol Identification Number
NCT03442400
Brief Title
A Prospective Study of Fractional Flow Reserve Assessment of Intermediate Coronary Stenoses in Severe Aortic Stenosis
Official Title
A Prospective Study of Fractional Flow Reserve Assessment of Intermediate Coronary Stenoses in Severe Aortic Stenosis
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Terminated
Why Stopped
Poor enrollment
Study Start Date
February 14, 2018 (Actual)
Primary Completion Date
August 10, 2021 (Actual)
Study Completion Date
August 10, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
The Cleveland Clinic
Collaborators
Volcano Corporation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Coronary artery blockages can reduce blood flow to the heart muscle. Fractional flow reserve (iFR or FFR) assessment is an invasive tool used to determine how much blood flow is reduced. The investigators will perform iFR/FFR on all intermediate coronary stenoses using standard practice, immediately before (at the time of) transcatheter aortic valve replacement (TAVR) and after successful TAVR. The investigators will compare pre- and post-TAVR iFR/FFR values, and assess short-term outcomes. The investigators hypothesize that iFR/FFR values will be consistently and significantly higher pre-TAVR in comparison with post-TAVR for the same lesions.
Detailed Description
The purpose of the study is to determine whether iFR assessment gives a valid assessment of coronary hemodynamics in patients with severe aortic stenosis. Several factors confound the interpretation of fractional flow reserve (FFR) in patients with severe aortic stenosis (AS) and intermediate severity coronary stenoses, and the widely accepted cut-off value of 0.80 may not be applicable to this patient population. Coronary flow reserve is known to be attenuated under conditions of left ventricular hypertrophy and severe AS, with one study showing improvement in coronary flow reserve after aortic valve replacement. Left ventricular hypertrophy produces fixed resistance secondary to external compression of the coronary microcirculation. This potentially results in failure to achieve maximal hyperemia with adenosine and can lead to false negative FFR results. Neurohormonal influences in aortic stenosis can further attenuate vasodilator response and potentially result in false negative FFR values. Both of these conditions result in the potential deferral of lesions which may have been hemodynamically significant in the absence of severe AS. At present, there are no studies which have demonstrated validity of FFR measurement in patients with severe AS. Here, the investigators propose a prospective study of iFR/FFR in patients with AS and indeterminate coronary lesions undergoing TAVR to understand the hemodynamic consequences of AS on iFR/FFR. The investigators hypothesize that iFR/FFR values will be consistently and significantly higher pre-TAVR in comparison with post-TAVR for the same lesions.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Stenoses, Aortic Stenosis
Keywords
Coronary Artery Stenoses, Aortic Stenosis

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
A single group of patients with severe aortic stenosis and intermediate coronary stenoses will undergo coronary physiology assessment with iFR/FFR before and after transcatheter aortic valve replacement.
Masking
None (Open Label)
Allocation
N/A
Enrollment
5 (Actual)

8. Arms, Groups, and Interventions

Arm Title
FFR/iFR arm
Arm Type
Experimental
Arm Description
Volcano iFR/FFR Verrata Plus coronary pressure/flow wire
Intervention Type
Device
Intervention Name(s)
Volcano iFR/FFR Verrata Plus coronary pressure/flow wire
Intervention Description
We will measure the degree of flow-limitation of intermediate severity coronary steonses using the iFR/FFR Verrata Plus coronary pressure/flow wire before and after transcatheter aortic valve replacement.
Primary Outcome Measure Information:
Title
FFR Values Prior to Transcatheter Aortic Valve Replacement
Description
Hemodynamic significance of a coronary stenosis by measuring FFR immediately prior to TAVR
Time Frame
Immediately prior to transcatheter aortic valve replacement, during the index procedure
Title
FFR Values During the Transcatheter Aortic Valve Replacement (TAVR)
Description
Hemodynamic significance of a coronary stenosis by measuring FFR immediately after TAVR
Time Frame
Immediately after transcatheter aortic valve replacement, during the index procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
110 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All patients who have coronary stenoses between 40-70% severity and who have severe aortic stenosis undergoing TAVR work-up. Exclusion Criteria: Patients with documented intraprocedural hemodynamic instability, shock, or major adverse event (myocardial infarction, aortic rupture/dissection, stroke, left ventricular perforation, cardiac arrest). Contraindication to adenosine, presence of cardiogenic shock, presence of acute coronary syndrome.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Samir R Kapadia, MD
Organizational Affiliation
The Cleveland Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
The Cleveland Clinic
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44195
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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A Prospective Study of Fractional Flow Reserve Assessment of Intermediate Coronary Stenoses in Severe Aortic Stenosis

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