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
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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RECRUITING
NA
50 participants
INTERVENTIONAL
2021-09-29
2025-09-30
Brief Summary
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Detailed Description
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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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Study Design
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NA
SINGLE_GROUP
DIAGNOSTIC
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.
Assession of complete coronary physiology
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.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* 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
* 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
18 Years
ALL
No
Sponsors
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Heart Center Leipzig - University Hospital
OTHER
Helios Health Institute GmbH
OTHER
Responsible Party
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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
Countries
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Central Contacts
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Mohamed Abdel-Wahab, Prof. Dr.
Role: CONTACT
Facility Contacts
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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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