Complete Functional Assessment of Intermediate Coronary Artery Stenosis Before and After Transcatheter Aortic Valve Implantation (TAVI) in Patients With Severe Symptomatic Aortic Valve Stenosis

NCT ID: NCT05133843

Last Updated: 2024-11-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-09-29

Study Completion Date

2025-09-30

Brief Summary

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The purpose of the current study is to assess complete coronary physiology (FFR, RFR, CFR, IMR, and CT-FFR) in TAVI candidates with intermediate coronary artery stenosis before and 6 months after TAVI. This aims to determine how TAVI affects coronary blood flow and coronary microcirculatory function after longer-term follow-up, and how these effects influence FFR and RFR values. In addition, it is aimed to correlate invasive functional testing (FFR and RFR) with non-invasive CT-FFR before and 6 months after TAVI.

Detailed Description

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Prospective, single center, open-label study to

1. compare coronary flow reserve (CFR), index of microvascular resistance (IMR), fractional flow reserve (FFR) and resting full cycle ratio (RFR) values before TAVI and 6 months after TAVI
2. correlate testing of microcirculatory function (IMR) with measurements of functional testing (FFR and RFR) before and six months after TAVI
3. correlate functional testing (FFR and RFR) with computed tomography (CT) derived fractional flow reserve (CT-FFR) before and six months after TAVI.

Conditions

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Coronary Artery Stenosis Transcatheter Aortic Valve Implantation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Prospective, single center, open-label
Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Coronary physiology

Assession of complete coronary physiology in TAVI candidates with intermediate coronary artery stenosis before and 6 months after TAVI.

Group Type OTHER

Assession of complete coronary physiology

Intervention Type PROCEDURE

Assession of complete coronary physiology in TAVI candidates with intermediate coronary artery stenosis before and 6 months after TAVI.

Interventions

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Assession of complete coronary physiology

Assession of complete coronary physiology in TAVI candidates with intermediate coronary artery stenosis before and 6 months after TAVI.

Intervention Type PROCEDURE

Other Intervention Names

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FFR, RFR, CFR, IMR, and CT-FFR

Eligibility Criteria

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Inclusion Criteria

* Age \>18 years
* Willing to participate and able to understand, read and sign the informed consent document before the planned procedure
* Severe symptomatic aortic stenosis with indication for TAVI according to current guidelines deemed by the Heart Team
* Patients who have undergone coronary CT angiography before TAVI in which CAD could not be ruled out
* CAD in one or more native major epicardial vessels or their branches by coronary angiogram with visually assessed coronary stenosis, in which the physiological severity of the lesion is in question (typically 40-90% diameter stenosis).
* Eligible for invasive coronary angiography and functional assessment (FFR, RFR, CFR and IMR)
* Eligible for coronary CT-angiography and functional assessment (CT-FFR)

Exclusion Criteria

* Patients whose CT-angiography was determined to be non-diagnostic/unreadable during its evaluation
* Previous coronary artery bypass grafting with patent grafts to the interrogated vessel
* Patients with severe lesions with a diameter stenosis ≥ 90%, flow-limiting lesions, or a significant left main coronary artery stenosis
* Critical coronary artery disease deemed by the Heart Team to require immediate revascularization
* Contraindication to adenosine (e.g. bronchial asthma)
* Chronic renal impairment with severe reduction of glomerular filtration rate (eGFR \<30 ml/min)
* Presence of cardiogenic shock
* Participation in another interventional study involving the left heart or coronary arteries
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Heart Center Leipzig - University Hospital

OTHER

Sponsor Role collaborator

Helios Health Institute GmbH

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Nicolas Majunke, Dr.

Role: STUDY_CHAIR

Heart Center Leipzig at University of Leipzig, Department of Internal Medicine/Cardiology

Robin Gohmann, Dr.

Role: PRINCIPAL_INVESTIGATOR

Heart Center Leipzig at University of Leipzig, Department of Internal Medicine/Cardiology

Mohamed Abdel-Wahab, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

Heart Center Leipzig at University of Leipzig, Department of Internal Medicine/Cardiology

Locations

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Heart Center Leipzig at University of Leipzig Department of Internal Medicine/Cardiology

Leipzig, , Germany

Site Status RECRUITING

Countries

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Germany

Central Contacts

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Nicolas Majunke, Dr.

Role: CONTACT

+49 341 865 1428

Mohamed Abdel-Wahab, Prof. Dr.

Role: CONTACT

Facility Contacts

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Nicolas Majunke, Dr.

Role: primary

+49 341 865 1428

Mohamed Abdel-Wahab, Prof. Dr.

Role: backup

Other Identifiers

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2021-0125

Identifier Type: -

Identifier Source: org_study_id

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